Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion wasGeneratedBy ECO_0000203 NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion wasDerivedFrom gad-20150221 NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion SIO_000772 12798584 NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion evidence source_evidence_literature NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.
- NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_assertion description "[Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67560.RA06QlUmfXgFNhzFxulqyMePdnK76h_oTcoSy21H47OvI130_provenance.