Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.
- NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_assertion description "[Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.
- NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_assertion evidence source_evidence_literature NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.
- NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_assertion SIO_000772 23708187 NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.
- NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_assertion wasDerivedFrom befree-20140225 NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.
- NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_assertion wasGeneratedBy ECO_0000203 NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP823342.RAq4TOi7dW_ujsWCzy8SnLIxabZKSUbDNgYM2q9ddzCMw130_provenance.