Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.
- NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_assertion wasGeneratedBy ECO_0000203 NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.
- NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_assertion wasDerivedFrom befree-20140225 NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.
- NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_assertion SIO_000772 20065966 NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.
- NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_assertion evidence source_evidence_literature NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.
- NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_assertion description "[Six tagSNPs, which capture all common genetic variation in the HTR2C gene, were genotyped in 4978 men and women from the European Prospective Investigation into Cancer (EPIC)-Norfolk study, an ongoing prospective population-based cohort study in the United Kingdom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP399002.RA0r6OaREvswXAQljso4cwaPhe-nip8fBfSRXqM9Q5tYg130_provenance.