Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.
- NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_assertion description "[Thus, CDKN2 deletions occur twice as commonly in GBM with EGFR amplification (71%) than in GBM with TP53 mutation (29%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.
- NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_assertion evidence source_evidence_literature NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.
- NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_assertion SIO_000772 9217972 NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.
- NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_assertion wasDerivedFrom gad-20130706 NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.
- NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_assertion wasGeneratedBy ECO_0000203 NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP45186.RA_3j-CYFBsrM1fEpZlNIqnQMpYpCgmreLqhqd14vpiLU130_provenance.