Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_assertion description "[In addition, we identified a non-synonymous variant in the NKX2-5 gene (P257A) associated with one congenital heart disease patient with VSD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_assertion evidence source_evidence_literature NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_assertion SIO_000772 20659440 NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_assertion wasDerivedFrom befree-20140225 NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_assertion wasGeneratedBy ECO_0000203 NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP397262.RABZHj76GBFNouC05z0QC-TV0ahqM4rwzgof4RFLMYB2Y130_provenance.