Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
- NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_assertion description "[Recent progress in the generation and characterization of transgenic mice expressing the genes containing expanded repeats associated with spinal and bulbar muscular atrophy (SBMA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD/SCA3), and Huntington's disease (HD) is beginning to provide insight into the underlying mechanisms of these neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
- NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_assertion evidence source_evidence_literature NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
- NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_assertion SIO_000772 9217978 NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
- NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_assertion wasDerivedFrom befree-20150227 NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
- NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_assertion wasGeneratedBy ECO_0000203 NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP557498.RA9QFiM5_RY0KLSdRTTNl4eUioDcduSKhlkGFv6e4v0vk130_provenance.