Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.
- NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_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." NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.
- NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_assertion evidence source_evidence_literature NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.
- NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_assertion SIO_000772 19651702 NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.
- NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_assertion wasDerivedFrom befree-20140225 NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.
- NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_assertion wasGeneratedBy ECO_0000203 NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP696573.RANwqrBeB0Ij5YAqGD3XunLU6Nv6fhlmF30pHWvmmutJA130_provenance.