Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.
- NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_assertion description "[Two molecular defects have been described in parathyroid adenomas: rearrangement and overexpression of the PRAD1/cyclin D1 oncogene and allelic loss of chromosome 11 DNA, often including the multiple endocrine neoplasia type 1 (MEN1) putative tumor suppressor gene region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.
- NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_assertion evidence source_evidence_literature NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.
- NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_assertion SIO_000772 7541648 NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.
- NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_assertion wasDerivedFrom befree-20140225 NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.
- NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_assertion wasGeneratedBy ECO_0000203 NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP807651.RAyzpW07G_ulAFc3QAOHVidRgmGTLsI9w7aRKWeo3ZNxU130_provenance.