Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.
- NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_assertion description "[Mosaicism for HOXA13 polyalanine expansions may be associated with a normal phenotype, making examination of parental DNA essential in apparently de novo HFGS cases to predict accurate recurrence risks.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.
- NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_assertion evidence source_evidence_literature NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.
- NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_assertion SIO_000772 23532960 NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.
- NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_assertion wasDerivedFrom befree-20140225 NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.
- NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_assertion wasGeneratedBy ECO_0000203 NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718902.RAC2OwQ_O4WlZ-BjtNZdyB_yR6wlVCGb5RFmZzzVVy84g130_provenance.