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- source_evidence_literature type ECO_0000212 NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.
- NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_assertion description "[The rise of next generation sequencing (NGS) and array-CGH (aCGH) in diagnostic settings for the evaluation of patients with ID allowed the identification of 17 patients carrying heterozygous genetic aberrations involving DYRK1A to date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.
- NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_assertion evidence source_evidence_literature NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.
- NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_assertion SIO_000772 25641759 NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.
- NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_assertion wasDerivedFrom befree-2016 NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.
- NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_assertion wasGeneratedBy ECO_0000203 NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260148.RAgta7gCx-jhz-a5APoDBYT--YUJo4rYOW-14PHR9-92A130_provenance.