Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.
- NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_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." NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.
- NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_assertion evidence source_evidence_literature NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.
- NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_assertion SIO_000772 19578791 NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.
- NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_assertion wasDerivedFrom befree-20150227 NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.
- NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_assertion wasGeneratedBy ECO_0000203 NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP277720.RAsseUBqUmggKkRT-Gd0tSXVHd4IZL7smw0_CfkaaJY8s130_provenance.