Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.
- NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_assertion description "[Germline mutations in the VHL gene cause dysregulation of HIF and induce an autosomal dominant cancer syndrome referred to as VHL disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.
- NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_assertion evidence source_evidence_literature NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.
- NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_assertion SIO_000772 16969113 NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.
- NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_assertion wasDerivedFrom befree-2016 NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.
- NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_assertion wasGeneratedBy ECO_0000203 NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.
- befree-2016 importedOn "2016-02-19" NP569044.RAkF6YXpzel0nQJ411f2_4RpArAWbVNdr5tj_k4NC99_A130_provenance.