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- NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_assertion type Assertion NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_head.
- NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_assertion wasGeneratedBy ECO_0000203 NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_provenance.
- NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_assertion wasDerivedFrom befree-20140225 NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_provenance.
- NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_assertion SIO_000772 20130826 NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_provenance.
- NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_assertion evidence source_evidence_literature NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_provenance.
- NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_assertion description "[Mutations in SOX10 are associated with several neurocristopathies such as Waardenburg syndrome type IV (WS4), a congenital disorder characterized by the association of hearing loss, pigmentary abnormalities, and absence of ganglion cells in the myenteric and submucosal plexus of the gastrointestinal tract, also known as aganglionic megacolon or Hirschsprung disease (HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516911.RAKOwbPuCdl8bhmetblOVTicKBsg5lu5OCSikr_qfhaDA130_provenance.