Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.
- NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_assertion description "[Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.
- NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_assertion evidence source_evidence_literature NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.
- NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_assertion SIO_000772 19221116 NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.
- NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_assertion wasDerivedFrom gad-20150221 NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.
- NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_assertion wasGeneratedBy ECO_0000203 NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP94940.RA1Jjezb0eiU3k5D6f6K3iBHNHMZuOIQjYv4FhI7EeMjM130_provenance.