Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.
- NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_assertion description "[Serious venous thromboembolism, heterozygous factor V Leiden and prothrombin G20210A mutations in a patient with Klinefelter syndrome and type 2 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.
- NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_assertion evidence source_evidence_literature NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.
- NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_assertion SIO_000772 19755774 NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.
- NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_assertion wasDerivedFrom befree-20150227 NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.
- NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_assertion wasGeneratedBy ECO_0000203 NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP389351.RAKmXJR8p8GWY1Tw0yHoY9_TD4rZUntl0iVb4ESXLgslY130_provenance.