Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.
- NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_assertion description "[FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.
- NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_assertion evidence source_evidence_literature NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.
- NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_assertion SIO_000772 10553987 NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.
- NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_assertion wasDerivedFrom befree-20140225 NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.
- NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_assertion wasGeneratedBy ECO_0000203 NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914281.RA8HEItf_9O643_diYVtrLxw0JIq7dxDOgPcSD25psQmw130_provenance.