Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.
- NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_assertion description "[In this study, the coding region of this gene and 1500 bp upstream of the 5'UTR has been sequenced in germline DNA in 192 PrCa patients with family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.
- NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_assertion evidence source_evidence_literature NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.
- NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_assertion SIO_000772 19997100 NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.
- NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_assertion wasDerivedFrom befree-20140225 NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.
- NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_assertion wasGeneratedBy ECO_0000203 NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP493154.RAmhmVZYXoYWHCKFe4-V8cME0pFzgDQM8jvOLJKgHdWcw130_provenance.