Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.
- NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_assertion description "[These iPSC models of genomic imprinting disorders will facilitate investigation of the AS and PWS disease processes and allow study of the developmental timing and mechanism of UBE3A repression in human neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.
- NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_assertion evidence source_evidence_literature NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.
- NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_assertion SIO_000772 20876107 NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.
- NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_assertion wasDerivedFrom befree-2016 NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.
- NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_assertion wasGeneratedBy ECO_0000203 NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.
- befree-2016 importedOn "2016-02-19" NP842148.RAnD2hCv3fJylxn0Pg-vnMg1PO-5nAXl-9CfiholL4TpU130_provenance.