Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.
- NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_assertion description "[The inherited deficiencies of protein C, protein S, antithrombin III, factor V Leiden mutation, prothrombin gene polymorphism, and antiphospholipids were studied in 53 Budd-Chiari syndrome (BCS) and 33 portal vein thrombosis (PVT) cases and compared with 223 age- and sex-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.
- NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_assertion evidence source_evidence_literature NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.
- NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_assertion SIO_000772 11584361 NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.
- NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_assertion wasDerivedFrom befree-20140225 NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.
- NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_assertion wasGeneratedBy ECO_0000203 NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP855180.RAAiRA-oRVJW3eVChwK5lAP7KsLhgocZeZ9cKShnyy4dY130_provenance.