Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.
- NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_assertion description "[These observations indicate that inactivating mutation of the p18 gene occurs uncommonly, if at all, in parathyroid adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.
- NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_assertion evidence source_evidence_literature NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.
- NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_assertion SIO_000772 9286748 NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.
- NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_assertion wasDerivedFrom befree-20150227 NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.
- NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_assertion wasGeneratedBy ECO_0000203 NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP967937.RAHDfDCykihYP3FTTBcz0anxNQe6lMiYKNttpel2TeX6Y130_provenance.