Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.
- NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_assertion description "[Candidate associations were identified between recurrent miscarriage and genetic variation within ESR2, PRLR, GCCR and ACVR1 genes. Independent confirmation of these results is needed, as limitations of this study include the heterogeneous etiology of rec]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.
- NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_assertion evidence source_evidence_literature NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.
- NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_assertion SIO_000772 20716560 NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.
- NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_assertion wasDerivedFrom gad-20150221 NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.
- NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_assertion wasGeneratedBy ECO_0000203 NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP146852.RABVtysKYSqTNPK0ik1Dtc1isHEZ7ixanpIRCOq6y__dQ130_provenance.