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- source_evidence_literature type ECO_0000212 NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.
- NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_assertion description "[A family history of ALS/PDC was recorded in more than 70% of patients, but no abnormal mutation or polymorphism was found in the genes of SOD1, tau, and apolipoprotein E. Familial nature and continuing morbidity of Kii ALS/PDC suggest that genetic factors may be more likely in its pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.
- NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_assertion evidence source_evidence_literature NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.
- NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_assertion SIO_000772 16092099 NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.
- NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_assertion wasDerivedFrom befree-2016 NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.
- NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_assertion wasGeneratedBy ECO_0000203 NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.
- befree-2016 importedOn "2016-02-19" NP508277.RACLuncNstmaJSPQlJ_MjCv1icphcabvwc3Rb_ECviWN0130_provenance.