Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.
- befree-2016 importedOn "2016-02-19" NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.
- NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_assertion wasGeneratedBy ECO_0000203 NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.
- NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_assertion wasDerivedFrom befree-2016 NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.
- NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_assertion SIO_000772 20832539 NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.
- NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_assertion evidence source_evidence_literature NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.
- NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_assertion description "[Compared with the entire cohort, the group with premalignant lesions demonstrated more p53 mutations (11% vs 50%; P = .004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838470.RA55PADby7YSl6Bzl-hMVxAii_EMQRDTg2lz2XnP7kNDE130_provenance.