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- source_evidence_literature type ECO_0000212 NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.
- NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_assertion description "[Mutations in the myelin protein zero (MPZ) gene have been associated with different Charcot-Marie-Tooth disease (CMT) phenotypes, including classical demyelinating CMT1B and the axonal form of the disease (CMT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.
- NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_assertion evidence source_evidence_literature NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.
- NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_assertion SIO_000772 19293842 NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.
- NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_assertion wasDerivedFrom befree-2016 NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.
- NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_assertion wasGeneratedBy ECO_0000203 NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.
- befree-2016 importedOn "2016-02-19" NP726749.RARPcWL3iSxNWxFAF6ssnYPUU3hEv87GhQWThCv0Wue68130_provenance.