Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.
- NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_assertion description "[However, rare kindreds with familial CCRCC (FCRC) not linked to the VHL tumour suppressor gene have been described suggesting that further familial RCC susceptibility genes exist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.
- NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_assertion evidence source_evidence_literature NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.
- NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_assertion SIO_000772 10807693 NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.
- NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_assertion wasDerivedFrom befree-2016 NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.
- NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_assertion wasGeneratedBy ECO_0000203 NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.
- befree-2016 importedOn "2016-02-19" NP283611.RAJz4RrDXxIQNvAtQZOYWYtf5iJD0dRARTlTRJb_it7nA130_provenance.