Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.
- NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_assertion description "[To detect chromosomal rearrangements indicating novel positional candidate RSTS genes, we used a-CGH to study 26 patients fulfilling the diagnostic criteria for RSTS who were negative at fluorescence in situ hybridisation analyses of the CREBBP and EP300 regions, and direct sequencing analyses of the CREBBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.
- NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_assertion evidence source_evidence_literature NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.
- NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_assertion SIO_000772 20125191 NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.
- NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_assertion wasDerivedFrom befree-20140225 NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.
- NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_assertion wasGeneratedBy ECO_0000203 NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP688701.RA4vOU49_gFfe1wPCHNlvYqBDOxje7IOLMrKPpAOHDkL8130_provenance.