Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.
- NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_assertion description "[The involvement of GJB2 in autosomal dominant deafness has also been proposed, although the putative mutation identified in one family with both deafness and palmoplantar keratoderma has recently been suggested to be merely a non-disease associated polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.
- NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_assertion evidence source_evidence_literature NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.
- NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_assertion SIO_000772 9856479 NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.
- NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_assertion wasDerivedFrom befree-20140225 NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.
- NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_assertion wasGeneratedBy ECO_0000203 NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP631111.RA9z5wUmeESuNdn60kZkqS83WqCKv9gYaQXxaLNjsiPBg130_provenance.