Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.
- NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_assertion description "[This showed that the two nuclear envelope defects (EDMD LMNA, EDMD emerin) were highly related disorders and were also related to fascioscapulohumeral muscular dystrophy (FSHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.
- NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_assertion evidence source_evidence_literature NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.
- NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_assertion SIO_000772 16478798 NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.
- NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_assertion wasDerivedFrom befree-20150227 NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.
- NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_assertion wasGeneratedBy ECO_0000203 NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537618.RAzlzZC4WsUpF1Ld3f2_DtVB1VyOh04DnQx8tas08ZP1o130_provenance.