Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.
- NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_assertion description "[RAB7 mutations were only found in patients with a Charcot-Marie-Tooth type 2B (CMT2B) phenotype, an axonal sensory-motor neuropathy with pronounced ulcero-mutilations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.
- NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_assertion evidence source_evidence_literature NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.
- NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_assertion SIO_000772 19651702 NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.
- NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_assertion wasDerivedFrom befree-2016 NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.
- NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_assertion wasGeneratedBy ECO_0000203 NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.
- befree-2016 importedOn "2016-02-19" NP755129.RA1CvXb6H2agRsNZBwFiwHwfx3YTWSMZBPUPynj8ljypE130_provenance.