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- source_evidence_literature type ECO_0000212 NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.
- NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_assertion description "[Dejerine-Sottas disease (DSD), also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile-onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene or the P0 gene and shares considerable clinical and pathological features with CMT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.
- NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_assertion evidence source_evidence_literature NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.
- NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_assertion SIO_000772 10219749 NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.
- NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_assertion wasDerivedFrom befree-2016 NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.
- NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_assertion wasGeneratedBy ECO_0000203 NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.
- befree-2016 importedOn "2016-02-19" NP251192.RAIar8yayyKeasQT41Ou2o5Up2K8EsPiWcbyqHyy7thZY130_provenance.