Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_assertion> ?p ?o ?g. }
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- NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_assertion type Assertion NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_head.
- 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.
- NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_assertion evidence source_evidence_literature NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_provenance.
- NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_assertion SIO_000772 8744027 NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_provenance.
- NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_assertion wasDerivedFrom befree-20140225 NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_provenance.
- NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_assertion wasGeneratedBy ECO_0000203 NP171573.RA0-d132wDFC-4XFavDdFBadq3z1n4VuzM0h4a34xpVRU130_provenance.