Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.
- NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_assertion description "[In contrast to oligodendrogliomas where CIC mutations were always detected along with 1p/19q co-deletion, CIC mutations were only found in 52 % of the 1p/19q co-deleted oligoastrocytomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.
- NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_assertion evidence source_evidence_literature NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.
- NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_assertion SIO_000772 22588899 NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.
- NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_assertion wasDerivedFrom befree-2016 NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.
- NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_assertion wasGeneratedBy ECO_0000203 NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.
- befree-2016 importedOn "2016-02-19" NP982546.RA_gtarjvIxNYM1PJUHXMBDa9yw2-bFCMu0IPkaPlX0iU130_provenance.