Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.
- NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_assertion description "[These disorders include deficiencies of anticoagulant proteins such as protein C, protein S, and antithrombin III, abnormalities of factor V and prothrombin resulting from genetic mutations, and hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.
- NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_assertion evidence source_evidence_literature NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.
- NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_assertion SIO_000772 18320477 NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.
- NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_assertion wasDerivedFrom befree-20140225 NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.
- NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_assertion wasGeneratedBy ECO_0000203 NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP595364.RAIlntO1Q3mN3NwuJyF1TKQG-eDDS7jZyecsHsrjPW-aQ130_provenance.