Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.
- NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_assertion description "[The aim of this case-control study was to investigate a number of acquired and inherited thrombophilic risk factors [antithrombin, protein C and S; factor V (FV) Leiden, FII polymorphism; lupus anticoagulant (LA); anticardiolipin (aCL) antibodies; fasting homocysteine (Hcy); lipoprotein(a) (Lp(a)); plasminogen activator inhibitor-1 (PAI-1)] in addition to cardiovascular risk factors in patients with idiopathic SSHL (ISSHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.
- NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_assertion evidence source_evidence_literature NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.
- NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_assertion SIO_000772 15869586 NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.
- NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_assertion wasDerivedFrom befree-20140225 NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.
- NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_assertion wasGeneratedBy ECO_0000203 NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP798567.RAwLlqNIirDevmTuRHK6zduUMj034yxpU7LXW7Glw1Fkw130_provenance.