Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.
- NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_assertion description "[Because MTS1/p16/CDKN2 and the homologous MTS2/p15 gene map to a region of chromosome 9p21, which is frequently deleted in malignant gliomas, we searched for lesions of these genes in primary biopsies of glioblastoma multiforme (GBM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.
- NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_assertion evidence source_evidence_literature NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.
- NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_assertion SIO_000772 7887443 NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.
- NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_assertion wasDerivedFrom befree-20150227 NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.
- NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_assertion wasGeneratedBy ECO_0000203 NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP306761.RAf3sGAH5m6a_nFKwVX5o2o7-TBaCOL_YRgauoKW_i8vM130_provenance.