Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.
- NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_assertion description "[We demonstrate that DRD2 polymorphisms -141Cdel, 3208G>T, TaqIB; DRD4 -521C>T and DAT1/SLC6A3 -1476T>G are associated with a two- to five-fold increased NSCLC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.
- NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_assertion evidence source_evidence_literature NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.
- NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_assertion SIO_000772 17175058 NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.
- NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_assertion wasDerivedFrom befree-20150227 NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.
- NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_assertion wasGeneratedBy ECO_0000203 NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP921751.RAq1fOVNZvs3IkQVhvMy0yAuUygAgZU1xxpep4F9JC2QI130_provenance.