Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.
- NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_assertion description "[For GSTM1 genotypes, the overall values (controls plus patients with thyroid cancer; no.= 335) indicated that the frequency of the null genotype was 49.85%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.
- NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_assertion evidence source_evidence_literature NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.
- NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_assertion SIO_000772 19169061 NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.
- NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_assertion wasDerivedFrom lhgdn-20090331 NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.
- NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_assertion wasGeneratedBy ECO_0000203 NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP177368.RA19E-Le-gsSlNjTgpDbuzwjiF4SJGFjMUPPcRI10r2qk130_provenance.