Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.
- NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_assertion description "[The data indicate that IDH1 mutation combined with either TP53 mutation or total 1p/19q loss is a frequent and early change in the majority of oligodendroglial tumors, diffuse astrocytomas, anaplastic astrocytomas, and secondary glioblastomas but not in primary glioblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.
- NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_assertion evidence source_evidence_literature NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.
- NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_assertion SIO_000772 19435942 NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.
- NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_assertion wasDerivedFrom gad-20150221 NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.
- NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_assertion wasGeneratedBy ECO_0000203 NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP120887.RA9EZtRnArgL30iRdOaDR1CgtPeBWNADW84VcOkpfM3vs130_provenance.