Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.
- NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_assertion description "[The entire NTF4 gene and the POAG-associated SNPs rs2156323 (VAV2) and rs2801219 (VAV3) and their flanking regions were screened by resequencing in a clinically well-characterized cohort of 537 subjects that included cases of POAG (n = 141), PACG (n = 111), and ethnically matched normal controls (n = 285).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.
- NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_assertion evidence source_evidence_literature NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.
- NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_assertion SIO_000772 20463313 NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.
- NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_assertion wasDerivedFrom befree-20150227 NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.
- NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_assertion wasGeneratedBy ECO_0000203 NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768214.RAmDYYyaUTDGIUtBsjlDU6VYSDB8yY-DtcEYRBwrNxDHc130_provenance.