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- source_evidence_literature type ECO_0000212 NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.
- NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_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." NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.
- NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_assertion evidence source_evidence_literature NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.
- NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_assertion SIO_000772 20716560 NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.
- NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_assertion wasDerivedFrom gad-20150221 NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.
- NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_assertion wasGeneratedBy ECO_0000203 NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP66657.RAUCXNlT0B_fOveyMeU6HGrfBCjAgzlinvoEUG5lPmlqI130_provenance.