Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.
- NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_assertion wasGeneratedBy ECO_0000218 NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.
- NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_assertion wasDerivedFrom uniprot-20150221 NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.
- NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_assertion SIO_000772 20711175 NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.
- NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_assertion evidence source_evidence_curated NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.
- NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_assertion description "[Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79.RApH9vYSjprma8h_0xyZlXuoExG3gVFbh1te2RTjykwcM130_provenance.