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- source_evidence_literature type ECO_0000212 NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.
- NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_assertion description "[Huntington's disease (HD) is a hereditary neurodegenerative disorder resulting from the expansion of a polyglutamine tract in the huntingtin protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.
- NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_assertion evidence source_evidence_literature NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.
- NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_assertion SIO_000772 22399227 NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.
- NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_assertion wasDerivedFrom befree-20150227 NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.
- NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_assertion wasGeneratedBy ECO_0000203 NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP445446.RAnDvahNR3fzBIZ4EmseHEqQ8S_mXb3s3-XN4pubvFNkA130_provenance.