Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.
- NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_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." NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.
- NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_assertion evidence source_evidence_literature NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.
- NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_assertion SIO_000772 7887443 NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.
- NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_assertion wasDerivedFrom befree-20140225 NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.
- NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_assertion wasGeneratedBy ECO_0000203 NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP265437.RAPqGt0dUpX0CeIDuj-kI7oXd1zzKVipGszH1CTNR0pp4130_provenance.