Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.
- befree-2016 importedOn "2016-02-19" NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.
- NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_assertion wasGeneratedBy ECO_0000203 NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.
- NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_assertion wasDerivedFrom befree-2016 NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.
- NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_assertion SIO_000772 8855829 NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.
- NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_assertion evidence source_evidence_literature NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.
- NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_assertion description "[Twenty-two patients with ovarian dysgenesis and a 566C-->T mutation in the FSH receptor gene (designated FSH-resistant ovaries or FSHRO) were compared with 30 clinically similar patients with ovarian dysgenesis (designated ODG) who did not have this mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1359759.RAwvCOoGmI_Rw1vsXvGLL09WcBXTeSU9bxnK4E-2lWric130_provenance.