Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424766.RAedvzed7tKow1IBgwHyrvPT1m25UwWkjh6_pvNFNdAxo130_provenance.
• NP200608.RANUNRsA4qe4eDfucxzLLZUCqUaJ0jJbM-ONoBiOn36j8130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200608.RANUNRsA4qe4eDfucxzLLZUCqUaJ0jJbM-ONoBiOn36j8130_provenance.
• NP240178.RAIz9MUFqCQoAqkAjHTOVwzN4iKAL7Pp62mOuiPFG6pxQ130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240178.RAIz9MUFqCQoAqkAjHTOVwzN4iKAL7Pp62mOuiPFG6pxQ130_provenance.
• NP227681.RAYhfrM2FwIZV41nANCd3h2OXfeNjMvrqxVVS5nq5Fz28130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227681.RAYhfrM2FwIZV41nANCd3h2OXfeNjMvrqxVVS5nq5Fz28130_provenance.
• NP864534.RAlSgNcf1Faq_pqELhXxPQhH0MwC4uDxg-vcU7LLunnCU130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864534.RAlSgNcf1Faq_pqELhXxPQhH0MwC4uDxg-vcU7LLunnCU130_provenance.
• NP443830.RAl-wweOXEK1NCac771dmKCxgzF9ZWDQ787udZdAyMfd8130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443830.RAl-wweOXEK1NCac771dmKCxgzF9ZWDQ787udZdAyMfd8130_provenance.
• NP599384.RAuoHgGc0FwtkI5e8c6BDxzn0E_ExlsDjz4WOxIK8EOWE130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599384.RAuoHgGc0FwtkI5e8c6BDxzn0E_ExlsDjz4WOxIK8EOWE130_provenance.
• NP627089.RAXMNPW4xjegN6lVKmtOQMQo354iFOTbn5cGqVm0bG7Qg130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627089.RAXMNPW4xjegN6lVKmtOQMQo354iFOTbn5cGqVm0bG7Qg130_provenance.
• NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_provenance.
• NP709739.RAcyx9jOBEzpXuW_fz5e-3hQd4YakKP1LhsUrTwmj_sgM130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709739.RAcyx9jOBEzpXuW_fz5e-3hQd4YakKP1LhsUrTwmj_sgM130_provenance.
• NP854395.RA3291jHK-_2RLw67tp8pYbN5R82xsSRxLnEAJx_A8OQ0130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854395.RA3291jHK-_2RLw67tp8pYbN5R82xsSRxLnEAJx_A8OQ0130_provenance.
• NP674509.RAQLdY0sYYDe3MVR___bsKHpL2OyR7PYCwtymaB1TAFaI130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674509.RAQLdY0sYYDe3MVR___bsKHpL2OyR7PYCwtymaB1TAFaI130_provenance.
• NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674530.RAYLpRRWmc-Z0m10T5lVOoZuuL3ZyL3zNOMiBuXzmUNKA130_provenance.
• NP619456.RAQJM2TxYfOT9f4bwuNaNs9iQqAXj7IzpBS9k2PizRtjk130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619456.RAQJM2TxYfOT9f4bwuNaNs9iQqAXj7IzpBS9k2PizRtjk130_provenance.
• assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354918.RAc0UWv6GZsMrhmddHIum4mxyLD0OPbmo6sAgVqDM4uAM130_provenance.
• NP1354919.RArtlRCfndXJyouH2lyu-37vx8BKtgHtHbRjty0cz_TyM130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354919.RArtlRCfndXJyouH2lyu-37vx8BKtgHtHbRjty0cz_TyM130_provenance.
• NP1354920.RAgRR7w9eQxHkO6E3jvZZV1Y5aEgLu23uMXls-Giwglkk130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354920.RAgRR7w9eQxHkO6E3jvZZV1Y5aEgLu23uMXls-Giwglkk130_provenance.
• NP619437.RA8Rtbg4Z7ww8D4sKFMpbGfrvTdxXSBaOCtB0ni2PWlCg130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619437.RA8Rtbg4Z7ww8D4sKFMpbGfrvTdxXSBaOCtB0ni2PWlCg130_provenance.
• NP619470.RAxmmrLREYsCnjDl9DHU1Ou_dVl6Rw4TnUZp6VpcbC5ik130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619470.RAxmmrLREYsCnjDl9DHU1Ou_dVl6Rw4TnUZp6VpcbC5ik130_provenance.
• NP1354916.RANLqCHTVpfOydvhXcY678JAW_0v2zQSfzOofWTFzhwyA130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354916.RANLqCHTVpfOydvhXcY678JAW_0v2zQSfzOofWTFzhwyA130_provenance.
• NP1354917.RA8Z7r_-xrRowrYU9w-F8Jf5TLI42okm8IWH-SE6c1zbc130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354917.RA8Z7r_-xrRowrYU9w-F8Jf5TLI42okm8IWH-SE6c1zbc130_provenance.
• NP1354921.RA1Wyk-1dsBtUFPkqE9OHKKNKpXnxqA_180PYQ5s6RPr0130_assertion description "[To facilitate the positional cloning of the genes involved in retinoschisis (RS), keratosis follicularis spinulosa decalvans (KFSD), Coffin-Lowry syndrome (CLS), X-linked hypophosphatemic rickets (XLH, locus name HYP) and X-linked dominant cone-rod degeneration (locus name RP15), we have extended the molecular map of the Xp22 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354921.RA1Wyk-1dsBtUFPkqE9OHKKNKpXnxqA_180PYQ5s6RPr0130_provenance.