Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.
- NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_assertion description "[We found a significantly higher frequency of AT1R 1166 C carriers (CC+AC) among the HCM patients without sarcomeric mutations compared to controls (p = 0.015; OR = 1.56; 95%CI = 1.09-2.23).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.
- NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_assertion evidence source_evidence_literature NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.
- NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_assertion SIO_000772 20594303 NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.
- NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_assertion wasDerivedFrom befree-20140225 NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.
- NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_assertion wasGeneratedBy ECO_0000203 NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624588.RA448mHZvHRVLEqZgL2oUomp01TYqV1G5HwGaDJqI3Qw0130_provenance.