Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.
- NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_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." NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.
- NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_assertion evidence source_evidence_literature NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.
- NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_assertion SIO_000772 23708187 NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.
- NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_assertion wasDerivedFrom befree-20140225 NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.
- NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_assertion wasGeneratedBy ECO_0000203 NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP436602.RApac8gkDbylqQm1ikZxCwFR7W-sosKdeaFcntTrT4GZU130_provenance.