Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.
- NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_assertion description "[Using expression microarrays and a unique method for comparative expression analysis called L2L, we sought to define this defect in cells lacking a functional CS group B (CSB) protein, the SWI/SNF-like ATPase responsible for most cases of CS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.
- NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_assertion evidence source_evidence_literature NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.
- NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_assertion SIO_000772 16772382 NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.
- NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_assertion wasDerivedFrom befree-20140225 NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.
- NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_assertion wasGeneratedBy ECO_0000203 NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173489.RAgydnZMX6y-JAVaAE2am4S-dHV-u1Q7M3pBjERv9epqo130_provenance.