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- source_evidence_literature type ECO_0000212 NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.
- NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_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." NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.
- NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_assertion evidence source_evidence_literature NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.
- NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_assertion SIO_000772 20384723 NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.
- NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_assertion wasDerivedFrom befree-20150227 NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.
- NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_assertion wasGeneratedBy ECO_0000203 NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978154.RA8pViNia1qmLCQxPaP-HO9su_sovHE6grKmhOFcDi82E130_provenance.