Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.
- NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_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." NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.
- NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_assertion evidence source_evidence_literature NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.
- NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_assertion SIO_000772 9286748 NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.
- NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_assertion wasDerivedFrom befree-20140225 NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.
- NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_assertion wasGeneratedBy ECO_0000203 NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP883755.RAN-kvncynUt6RXcnPfreGXlPgYbRDRVg-_PccTK0p75E130_provenance.