Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.
- NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_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." NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.
- NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_assertion evidence source_evidence_literature NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.
- NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_assertion SIO_000772 20716560 NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.
- NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_assertion wasDerivedFrom gad-20150221 NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.
- NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_assertion wasGeneratedBy ECO_0000203 NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP146853.RAA4nEq7w-ahUe-E7-uE7cF2ENxdBre_TsmJpfzuYLFJM130_provenance.