Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.
- befree-20150227 importedOn "2015-02-27" NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.
- NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_assertion wasGeneratedBy ECO_0000203 NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.
- NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_assertion wasDerivedFrom befree-20150227 NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.
- NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_assertion SIO_000772 21694734 NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.
- NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_assertion evidence source_evidence_literature NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.
- NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_assertion description "[Finally, we provide evidence that ISS in deletion 1p36 may be associated with deletion of KLHL17 and expand the epilepsy phenotype in that syndrome to include early infantile epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985576.RAzJV9roxs7FBCV_4Wl62BWP6NvIWoPSgH57qs_Ye3c28130_provenance.