Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.
- NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_assertion description "[In a case-control study, we also tested whether a variant adenine allele in the promoter polymorphism -161C-->A with a putative influence on the transcriptional activity of CDH1 in vitro confers any detectable risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.
- NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_assertion evidence source_evidence_literature NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.
- NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_assertion SIO_000772 11857408 NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.
- NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_assertion wasDerivedFrom befree-20140225 NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.
- NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_assertion wasGeneratedBy ECO_0000203 NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP351895.RAbp6eXUPe9sxo9oJe1sUD1w6_pHKD7zuME_ViXEyA3fU130_provenance.