Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.
- NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_assertion description "[We investigated three RAS gene polymorphisms--the ACE insertion/deletion (I/D), angiotensinogen (AGT) M235T, and angiotensin II type 1 receptor (AT1R) A1166C polymorphisms--for a possible role in modulating these disorders in 853 Chinese subjects with varying components of the metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.
- NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_assertion evidence source_evidence_literature NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.
- NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_assertion SIO_000772 11213892 NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.
- NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_assertion wasDerivedFrom befree-20140225 NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.
- NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_assertion wasGeneratedBy ECO_0000203 NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP771052.RAEDxOG_8Y4MWwo-OqZvHjE8BPEhe0kAxYfdUdhHIw0dY130_provenance.