Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_assertion> ?p ?o ?g. }
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- NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_assertion type Assertion NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_head.
- NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_assertion description "[BOR syndrome is an autosomal dominant trait encompassing branchial, otic and renal anomalies because of mutations in EYA1, SIX1 and SIX5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_provenance.
- NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_assertion evidence source_evidence_literature NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_provenance.
- NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_assertion SIO_000772 18177466 NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_provenance.
- NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_assertion wasDerivedFrom befree-20150227 NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_provenance.
- NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_assertion wasGeneratedBy ECO_0000203 NP388557.RA8Bed1MtYipaxFcjkoKP8Kixipw4_EGSSm7LqVW6Sb3M130_provenance.