Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.
- NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_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." NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.
- NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_assertion evidence source_evidence_literature NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.
- NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_assertion SIO_000772 9286748 NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.
- NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_assertion wasDerivedFrom befree-20140225 NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.
- NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_assertion wasGeneratedBy ECO_0000203 NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP547689.RAHe17xsNeCvNr6XhKzTKfgU2ThdWjatKbVHLAcDzAIEA130_provenance.