Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.
- NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_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." NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.
- NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_assertion evidence source_evidence_literature NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.
- NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_assertion SIO_000772 20716560 NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.
- NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_assertion wasDerivedFrom gad-20150221 NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.
- NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_assertion wasGeneratedBy ECO_0000203 NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP149983.RAlz_0D6sDbB2_HMZwNT5OnbJqrfT7sbTUXqYEhC--SDE130_provenance.