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- NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_assertion type Assertion NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_head.
- NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_assertion description "[Like the adult form of the disorder, JHD is a hereditary neurodegenerative disease characterized by dementia and behavioral changes, caused by an expanded CAG repeat within the first exon of the huntingtin (HTT) gene on chromosome 4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_provenance.
- NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_assertion evidence source_evidence_literature NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_provenance.
- NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_assertion SIO_000772 23390171 NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_provenance.
- NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_assertion wasDerivedFrom befree-20140225 NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_provenance.
- NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_assertion wasGeneratedBy ECO_0000203 NP870870.RALeMy0yrw8T_Lm20jATBEB_k_5gnijl_lQGW9aNc8fZk130_provenance.