Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.
- NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_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." NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.
- NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_assertion evidence source_evidence_literature NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.
- NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_assertion SIO_000772 20716560 NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.
- NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_assertion wasDerivedFrom gad-20150221 NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.
- NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_assertion wasGeneratedBy ECO_0000203 NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP148902.RAyhLKx37dXWdJLwUwdVcC0x5J4xk2xx4L6j08armawOs130_provenance.