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- source_evidence_literature type ECO_0000212 NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_assertion description "[Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_assertion evidence source_evidence_literature NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_assertion SIO_000772 18379723 NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_assertion wasDerivedFrom befree-20140225 NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_assertion wasGeneratedBy ECO_0000203 NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.