Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.
- NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_assertion description "[Mutations have been identified in alpha-tropomyosin (Tm), a key regulatory protein in striated muscle cells, that are associated with a human cardiac myopathy, hypertrophic cardiomyopathy (FHC) and a human skeletal myopathy, nemaline myopathy (NM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.
- NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_assertion evidence source_evidence_literature NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.
- NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_assertion SIO_000772 11199327 NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.
- NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_assertion wasDerivedFrom befree-2016 NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.
- NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_assertion wasGeneratedBy ECO_0000203 NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.
- befree-2016 importedOn "2016-02-19" NP308201.RAAbC5izDN7Q0Yz1ECljCk0o0JnYU4xqSw3DnxPt1a6Os130_provenance.