Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.
- NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_assertion wasGeneratedBy ECO_0000203 NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.
- NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_assertion wasDerivedFrom befree-20140225 NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.
- NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_assertion SIO_000772 23171239 NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.
- NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_assertion evidence source_evidence_literature NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.
- NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_assertion description "[Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP506854.RAyw2yixA3YWVCPx_vMkqVXe4U4MyOE3tNbGGDR2gz6Gg130_provenance.