Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.
- NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_assertion description "[The HDAC4 (2q37.2) variant rs73000144 (OR = 14.6, p = 0.018) and the EFCAB13 (17q21.3) variant rs118004742 (OR = 1.8, p = 0.048) were overrepresented in patients with familial PrCa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.
- NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_assertion evidence source_evidence_literature NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.
- NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_assertion SIO_000772 25335771 NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.
- NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_assertion wasDerivedFrom befree-2016 NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.
- NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_assertion wasGeneratedBy ECO_0000203 NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231312.RA_e_2yrm5b-tfYIYIKszAxuulFSH0cMKaug2qGcT84EY130_provenance.