Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.
- NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_assertion description "[A decrease in CAD patients carrying the CAC haplotype compared to controls (p=0.043) and a decrease in the CAC haplotype in CAD patients with hypertension vs healthy controls (p=0.029) were demonstrated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.
- NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_assertion evidence source_evidence_literature NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.
- NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_assertion SIO_000772 19578791 NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.
- NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_assertion wasDerivedFrom befree-20140225 NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.
- NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_assertion wasGeneratedBy ECO_0000203 NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718821.RAOztqa82uan0DuEHLxjkZkLH_o771poci5Qk0QcuSaAw130_provenance.