Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.
- NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_assertion description "[IDH mutations in gliomas are associated with several clinically relevant parameters including patient age, histopathological diagnosis, combined 1p/19q deletion, TP53 mutation, MGMT promoter hypermethylation and patient survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.
- NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_assertion evidence source_evidence_literature NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.
- NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_assertion SIO_000772 21955925 NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.
- NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_assertion wasDerivedFrom befree-2016 NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.
- NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_assertion wasGeneratedBy ECO_0000203 NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP927115.RAb22Ku8yz6B79IOlHzsrkTNgjC0uB7dvsjYkFZSYjMkQ130_provenance.