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- source_evidence_literature type ECO_0000212 NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.
- NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_assertion description "[Huntington disease (HD) is a fully penetrant, autosomal dominantly inherited disorder associated with abnormal expansions of a stretch of perfect CAG repeats in the 5' part of the IT15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.
- NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_assertion evidence source_evidence_literature NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.
- NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_assertion SIO_000772 16372906 NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.
- NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_assertion wasDerivedFrom befree-2016 NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.
- NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_assertion wasGeneratedBy ECO_0000203 NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.
- befree-2016 importedOn "2016-02-19" NP528138.RA6GelnEUq-PBU-PZSLRsk62l5fo39uH8wzS10cVQLWIE130_provenance.