Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.
- befree-2016 importedOn "2016-02-19" NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.
- NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_assertion wasGeneratedBy ECO_0000203 NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.
- NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_assertion wasDerivedFrom befree-2016 NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.
- NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_assertion SIO_000772 10414451 NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.
- NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_assertion evidence source_evidence_literature NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.
- NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_assertion description "[APC-R was observed to be the commonest defect underlying the Indian DVT as seen in 39.2% of patients followed by elevated ACA (5.3%), PAI (2.8%), presence of LA (2.8%) and reduced ATIII levels (2.8%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258175.RAbu8WsF8v5iMYMgnKcaOQWMxm2Ap6syA9Vj1NxRChvtM130_provenance.