Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.
- NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_assertion description "[A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.
- NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_assertion evidence source_evidence_literature NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.
- NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_assertion SIO_000772 20631719 NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.
- NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_assertion wasDerivedFrom befree-20140225 NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.
- NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_assertion wasGeneratedBy ECO_0000203 NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP525129.RA6A_Wmc6HYFB1BP1KDkO_b-Ccws443Ln5i_zxmnIChNs130_provenance.