Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.
- NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_assertion wasGeneratedBy ECO_0000203 NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.
- NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_assertion wasDerivedFrom befree-20150227 NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.
- NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_assertion SIO_000772 12176944 NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.
- NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_assertion evidence source_evidence_literature NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.
- NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_assertion description "[Given the association between CVD and PXE, we hypothesized that heterozygosity of this ABCC6 mutation could also confer an increased risk for CVD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251241.RAaUDYH7hQxi_Hzw2EoMi8ywNiXi9hQdnVxLupml5TuXo130_provenance.