Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.
- NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_assertion description "[No mutations were found in exon 2 of MTS2/p15 (12 cases examined), and one GBM showed a DNA deletion breakpoint in the 30 kb between MTS1/p16/CDKN2 and MTS2/p15 resulting in deletion of MTS1/p16/CDKN2 with retention of MTS2/p15.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.
- NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_assertion evidence source_evidence_literature NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.
- NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_assertion SIO_000772 7887443 NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.
- NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_assertion wasDerivedFrom befree-20140225 NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.
- NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_assertion wasGeneratedBy ECO_0000203 NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP270643.RA_RruRB4To-h4SWB7taNWymPro2AyoJ_YXgKQvi4bNNY130_provenance.