Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.
- NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_assertion description "[Interaction of MEF2C with the deleted febrile seizure (FEB4) and juveline myoclonic epilepsy (EJM4) loci plus the G-protein receptor (GPR98/MASS1/Usher syndrome) gene may moderate the phenotype, perhaps through common regulation by calcium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.
- NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_assertion evidence source_evidence_literature NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.
- NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_assertion SIO_000772 21567930 NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.
- NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_assertion wasDerivedFrom befree-20140225 NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.
- NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_assertion wasGeneratedBy ECO_0000203 NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP742109.RAesZMHiFNQgA2Hl7JOCXnRGWKju4PPCrMWpJ9ND8Ko1I130_provenance.