Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.
- NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_assertion description "[Hence, GLUD1 mutational analysis may be indicated in patients with leucine sensitivity; even in the absence of HA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.
- NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_assertion evidence source_evidence_literature NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.
- NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_assertion SIO_000772 19690084 NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.
- NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_assertion wasDerivedFrom befree-20150227 NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.
- NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_assertion wasGeneratedBy ECO_0000203 NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP429038.RAVm82qaDNS2v8ELfogmkNXXspLBuMVmoYKmGHzh-qitk130_provenance.