Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion description "[Usher syndromeIb (USH1B), an autosomal recessive disorder caused by mutations in myosin VIIa (MYO7A), is characterized by congenital profound hearing loss, vestibular abnormalities and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion evidence source_evidence_literature NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion SIO_000772 10612833 NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion wasDerivedFrom befree-2016 NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_assertion wasGeneratedBy ECO_0000203 NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.
- befree-2016 importedOn "2016-02-19" NP271069.RAUf76UaGX2D7CzqRqAwP4lz3hmJhSPPUniWVRzp-t-gU130_provenance.