Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.
- NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_assertion description "[Nine patients belonging to this kindred underwent coagulation study for hereditary thrombophilia, which included plasminogen antigen and activity assays, an activated protein C resistance test, and genetic analysis for factor V Leiden mutation and for prothrombin variant 20210A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.
- NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_assertion evidence source_evidence_literature NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.
- NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_assertion SIO_000772 10726047 NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.
- NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_assertion wasDerivedFrom befree-20140225 NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.
- NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_assertion wasGeneratedBy ECO_0000203 NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP927419.RANBe2UEjrMYKqxWBTd_DSXegNv9toJPXhsXtHZTF2qBY130_provenance.