Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.
- NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_assertion description "[The SDF-1 homozygous 3'A variant was related to more-rapid disease progression, and CCR5 Delta32 was associated with reduced rates of hazard for disease progression in nucleoside-treated subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.
- NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_assertion evidence source_evidence_literature NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.
- NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_assertion SIO_000772 11709782 NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.
- NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_assertion wasDerivedFrom gad-20150221 NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.
- NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_assertion wasGeneratedBy ECO_0000203 NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.
- gad-20150221 importedOn "2015-02-21" NP57167.RA_YJCNRPRGE4NhExyJrRytUU4gH6VLQKYM63M3duFx0o130_provenance.