Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_assertion> ?p ?o ?g. }
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- NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_assertion type Assertion NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_head.
- NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_assertion wasGeneratedBy ECO_0000218 NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_provenance.
- NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_assertion wasDerivedFrom uniprot-2016 NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_provenance.
- NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_assertion SIO_000772 14684684 NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_provenance.
- NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_assertion evidence source_evidence_curated NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_provenance.
- NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_assertion description "[A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3163.RAwW2K4GUKNlGFjuAFdNaYWyEhSJFVUZjNGOrCqF_orQc130_provenance.