Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.
- NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_assertion wasGeneratedBy ECO_0000203 NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.
- NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_assertion wasDerivedFrom befree-2016 NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.
- NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_assertion SIO_000772 23024041 NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.
- NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_assertion evidence source_evidence_literature NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.
- NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_assertion description "[Mutations in planar cell polarity (PCP) genes in mice cause a variety of defects including the NTD, craniorachischisis, and sometimes SB or exencephaly (EX); they also demonstrate the role of digenic combinations of PCP mutants in NTDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1016686.RA2B4HZIx2yvWlAFW8Boy4jgouFETNS61Ki9bShx8hhtA130_provenance.