Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.
- NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_assertion description "[The results showed the frequency of the Asp299Gly genotype was increased in patients with chronic disease (OR 25.3, 95% CI 5.2-115.6, P�<�0.001) and patients with acute disease (OR 8.03, 95% CI 1.7-37.7, P�=�0.006) compared to LST negative subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.
- NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_assertion evidence source_evidence_literature NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.
- NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_assertion SIO_000772 21056683 NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.
- NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_assertion wasDerivedFrom befree-20150227 NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.
- NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_assertion wasGeneratedBy ECO_0000203 NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.
- befree-20150227 importedOn "2015-02-27" NP990851.RAyALPuDD4D2tvLqH4zKtrOXvCmxteMxzeMfRQrqLmS80130_provenance.