Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.
- NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_assertion description "[No germline mutations were detected in the VHL or MET genes, suggesting that FCRC is not allelic with VHL disease or HPRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.
- NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_assertion evidence source_evidence_literature NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.
- NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_assertion SIO_000772 10807693 NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.
- NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_assertion wasDerivedFrom befree-20150227 NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.
- NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_assertion wasGeneratedBy ECO_0000203 NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP553995.RATUCjkULXYq2di0jWfNtMZTL83LQk3J1JBLo_OC4qgIg130_provenance.