Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_assertion description "[Currently, MHA, SBS, FTNS and EPS are considered to be distinct clinical manifestation of a single illness caused by mutations of the MYH9 gene encoding the heavy chain of non-muscle myosin IIA (NMMHC-IIA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_assertion evidence source_evidence_literature NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_assertion SIO_000772 18925516 NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_assertion wasDerivedFrom befree-20140225 NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_assertion wasGeneratedBy ECO_0000203 NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP505046.RAFSzlhQWpfrRUTCisHKEeLZtcP_dbtmClO5ycvQDxrFA130_provenance.