Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.
- NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_assertion description "[Clinically, the phaeochromocytoma-paraganglioma syndrome is often unrecognised, although 10-30% of apparently sporadic phaeochromocytomas and paragangliomas harbour germline SDH-gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.
- NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_assertion evidence source_evidence_literature NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.
- NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_assertion SIO_000772 19576851 NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.
- NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_assertion wasDerivedFrom befree-20140225 NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.
- NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_assertion wasGeneratedBy ECO_0000203 NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP351581.RA1UQwpm2WBs7UcjskQg6peyzPCjqqgnKiqeSTrt4ispk130_provenance.