Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.
- NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_assertion wasGeneratedBy ECO_0000203 NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.
- NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_assertion wasDerivedFrom befree-20150227 NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.
- NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_assertion SIO_000772 11550302 NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.
- NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_assertion evidence source_evidence_literature NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.
- NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_assertion description "[Loss of 9p or homozygous deletion of the CDKN2 gene or both are associated with anaplastic oligodendrogliomas, whereas loss of 17p or TP53 gene mutations or both are frequent in astrocytomas, but rare in oligodendrogliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300809.RAp2ILJe1BmLj7ALLs5hD-cQN2jH603O7RJNSMziWvomA130_provenance.