Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.
- NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_assertion wasGeneratedBy ECO_0000203 NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.
- NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_assertion wasDerivedFrom befree-20140225 NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.
- NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_assertion SIO_000772 22846739 NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.
- NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_assertion evidence source_evidence_literature NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.
- NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_assertion description "[The primary syndromes (and genes) addressed here include multiple endocrine neoplasia types 1 and 2 (MEN1 and RET genes), Cowden syndrome (PTEN), hereditary pheochromocytoma/paraganglioma syndromes (multiple genes), and von Hippel-Lindau disease (VHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP533835.RAZuZG9Fe02krQBfUIet2Fwl_Rxkml8oTrsopnPKbvm5A130_provenance.