Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.
- NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_assertion description "[Taken together, our findings supported a positive association between OPRD1 variants and SD, and a positive haplotypic association between OPRK1 and AD in EAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.
- NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_assertion evidence source_evidence_literature NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.
- NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_assertion SIO_000772 17622222 NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.
- NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_assertion wasDerivedFrom befree-20140225 NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.
- NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_assertion wasGeneratedBy ECO_0000203 NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP453065.RAYoRB9XCco8N0ErJe2ruqxcGU1mZ8SNfw8Phrtfk7EXw130_provenance.