Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.
- NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_assertion wasGeneratedBy ECO_0000203 NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.
- NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_assertion wasDerivedFrom befree-20150227 NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.
- NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_assertion SIO_000772 12798584 NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.
- NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_assertion evidence source_evidence_literature NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.
- NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_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." NP334074.RAnvn8i8rWU2Ip0WpbH3bpLiNaFTVanCymBQRHiPhQU_I130_provenance.