Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.
- NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_assertion description "[They include at least nine disorders, including Huntington's disease (HD), dentatorubral pallidoluysian atrophy (DRPLA), spinal and bulbar muscular atrophy (SBMA), and the spinocerebellar ataxias SCA1, SCA2, SCA3 (also known as Machado-Joseph disease), SCA6, SCA7, and SCA17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.
- NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_assertion evidence source_evidence_literature NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.
- NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_assertion SIO_000772 17786457 NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.
- NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_assertion wasDerivedFrom befree-20150227 NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.
- NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_assertion wasGeneratedBy ECO_0000203 NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681712.RANR5IwdXq9Lzm-Q_oyqObm4K5xBav4R2m_IpP2vjZFFM130_provenance.