Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.
- NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_assertion description "[These results suggest that GYLTL1B may be a candidate gene for muscular dystrophy and that its overexpression could compensate for the deficiency of both LARGE and other glycosyltransferases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.
- NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_assertion evidence source_evidence_literature NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.
- NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_assertion SIO_000772 15661757 NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.
- NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_assertion wasDerivedFrom befree-20140225 NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.
- NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_assertion wasGeneratedBy ECO_0000203 NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722999.RAAMRWgkdVMK18mf51MZRWwzLUb2uHYdGp9NNtqnIc-nQ130_provenance.