Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.
- NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_assertion description "[Rare cases have been reported in von Hippel-Lindau (VHL) patients (germline mutation of the VHL gene), the significance of which is uncertain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.
- NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_assertion evidence source_evidence_literature NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.
- NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_assertion SIO_000772 23648463 NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.
- NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_assertion wasDerivedFrom befree-2016 NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.
- NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_assertion wasGeneratedBy ECO_0000203 NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1075384.RAgNQWUKeCx4Vg3qfQQf0J_Ooc04n3rHIrRIdcPxASPyY130_provenance.