Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.
- NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_assertion description "[We report somatic heterozygous mutations in IDH1 (c.394C>T encoding an R132C substitution and c.395G>A encoding an R132H substitution) or IDH2 (c.516G>C encoding R172S) in 87% of enchondromas (benign cartilage tumors) and in 70% of spindle cell hemangiomas (benign vascular lesions).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.
- NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_assertion evidence source_evidence_literature NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.
- NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_assertion SIO_000772 22057234 NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.
- NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_assertion wasDerivedFrom befree-20140225 NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.
- NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_assertion wasGeneratedBy ECO_0000203 NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563633.RAxAPlUITnAq-en-crgHw9AqSQEkSyIAsTrMRDtkriKBs130_provenance.