Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.
- NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_assertion description "[Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.
- NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_assertion evidence source_evidence_literature NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.
- NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_assertion SIO_000772 19578366 NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.
- NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_assertion wasDerivedFrom gad-20150221 NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.
- NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_assertion wasGeneratedBy ECO_0000203 NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151800.RA9FdWi0UQ17wSNfRNqE7bScRJ_-ECkw2wXOYjOr2ovmU130_provenance.