Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.
- NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_assertion description "[Candidate associations were identified between recurrent miscarriage and genetic variation within ESR2, PRLR, GCCR and ACVR1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.
- NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_assertion evidence source_evidence_literature NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.
- NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_assertion SIO_000772 20716560 NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.
- NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_assertion wasDerivedFrom gad-20150221 NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.
- NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_assertion wasGeneratedBy ECO_0000203 NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP183791.RA5FLxHigZ_FnQO4Vy0lQ1pvpAYkkVHpinV1fWaId10Z0130_provenance.