Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.
- NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_assertion description "[Recently, longer expansion of the first polyalanine tract of ARX was found to be causative for Ohtahara syndrome without brain malformation, whereas premature termination mutations of ARX were found to cause severe brain malformations, such as lissencephaly or hydranencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.
- NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_assertion evidence source_evidence_literature NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.
- NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_assertion SIO_000772 20384723 NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.
- NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_assertion wasDerivedFrom befree-20140225 NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.
- NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_assertion wasGeneratedBy ECO_0000203 NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP896214.RAtQZ2URsvvscqCs0K0YVfe7IOsycMM_xm0O9fx6A25tc130_provenance.