Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.
- NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_assertion description "[To describe the phenotypic spectrum and genetics of periventricular nodular heterotopia (PNH) caused by FLN1 mutations in four men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.
- NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_assertion evidence source_evidence_literature NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.
- NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_assertion SIO_000772 15249610 NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.
- NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_assertion wasDerivedFrom befree-20140225 NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.
- NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_assertion wasGeneratedBy ECO_0000203 NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP577524.RAFJe1I9i84H-oSWmCS1hSsiPbfgnlR-7YNLXMxdLt-Fo130_provenance.