Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.
- NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_assertion description "[We explored a new candidate gene, APOA5, for possible causative mutations in a pedigree of late-onset, vertically transmitted hyperchylomicronemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.
- NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_assertion evidence source_evidence_literature NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.
- NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_assertion SIO_000772 16200213 NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.
- NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_assertion wasDerivedFrom befree-20140225 NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.
- NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_assertion wasGeneratedBy ECO_0000203 NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP663880.RAJC5dgKPOwlObtekFAlzuWUrde_VKQDv--moAJGaq8dw130_provenance.