Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.
- NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_assertion description "[Various studies have demonstrated that factor V Leiden (FVL) and G20210A prothrombin mutation contribute to the risk of Budd-Chiari syndrome (BCS), while other studies provided conflicting findings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.
- NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_assertion evidence source_evidence_literature NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.
- NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_assertion SIO_000772 24755609 NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.
- NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_assertion wasDerivedFrom befree-20150227 NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.
- NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_assertion wasGeneratedBy ECO_0000203 NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP391756.RA8d6lXTAq2NuNCiWV_2F7eTBe-UUiQ8YN4PuAcuR03JI130_provenance.