Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.
- NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_assertion description "[We examined the prevalence of factor V Leiden, the prothrombin G20210A genotype, and the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in 100 patients (51 males and 49 females) who survived an ischemic stroke without a cardiac embolic source at an age < or = 45 years, and in 238 healthy control subjects from the same geographic area.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.
- NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_assertion evidence source_evidence_literature NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.
- NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_assertion SIO_000772 11697722 NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.
- NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_assertion wasDerivedFrom befree-20140225 NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.
- NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_assertion wasGeneratedBy ECO_0000203 NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP446055.RAv4q-mOR2op_Z-rChHiNs7_CcXqPDySpLENLlFqAstYA130_provenance.