Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.
- NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_assertion wasGeneratedBy ECO_0000203 NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.
- NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_assertion wasDerivedFrom lhgdn-20090331 NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.
- NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_assertion SIO_000772 18184292 NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.
- NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_assertion evidence source_evidence_literature NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.
- NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_assertion description "[D999H is a novel Hemiplegic Migraine, Familial ATP1A2 mutation in an Irish family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP142197.RAfRQOxFN5DiDcB0uUNC7llQFz2fchLtD9rqeOgxdmikY130_provenance.