Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
• NP740336.RApYxyuoH4W9fK_oLpao9ci-0MSt_kQFZHGGPVXAOydwc130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740336.RApYxyuoH4W9fK_oLpao9ci-0MSt_kQFZHGGPVXAOydwc130_provenance.
• assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364288.RAfEQUgRHl7jttfRhnK2bT2vAf7Eol1QEMMKHh4lECfNg130_provenance.
• NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763329.RA4t-6rjl2qzrdd4F9C-KHD3cdYbBbxiuNpnvojpVdxIY130_provenance.
• NP631920.RAKdzWMRlNWYwU3KgLclUwjNo-kws4hdMGZao8g5jRjYg130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631920.RAKdzWMRlNWYwU3KgLclUwjNo-kws4hdMGZao8g5jRjYg130_provenance.
• NP20663.RAVo5cLiAk7dcY39sizqfDghfZSBVTIu6zxien9VXaHS8130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20663.RAVo5cLiAk7dcY39sizqfDghfZSBVTIu6zxien9VXaHS8130_provenance.
• NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
• NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_provenance.
• NP938237.RA7L5KL81Zr0Jn8xR7bWMXZr2BbXUzHyiVSN2fCZx_k1s130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938237.RA7L5KL81Zr0Jn8xR7bWMXZr2BbXUzHyiVSN2fCZx_k1s130_provenance.