Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.
- NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_assertion wasGeneratedBy ECO_0000203 NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.
- NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_assertion wasDerivedFrom gad-20150221 NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.
- NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_assertion SIO_000772 17600229 NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.
- NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_assertion evidence source_evidence_literature NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.
- NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_assertion description "[The previously observed association with the IL4R 503 S/P variant and the novel association with the LTC4S(-444) A/C variant suggest that these loci may also contribute to large vessel stroke risk in children with SCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP108675.RAwre6HRtHnLeChdW-_pS76Jf0q2VZCBxAgtP5M73Pq-8130_provenance.