Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.
- NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_assertion description "[Huntington disease (HD) is a neurodegenerative disorder caused by the expansion of a polyglutamine tract in the huntingtin (htt) protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.
- NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_assertion evidence source_evidence_literature NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.
- NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_assertion SIO_000772 21044956 NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.
- NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_assertion wasDerivedFrom befree-2016 NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.
- NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_assertion wasGeneratedBy ECO_0000203 NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.
- befree-2016 importedOn "2016-02-19" NP849999.RAdD0KtzpgVg72MCxE_TdgCcV4j8XO1eC1Eh86684hqU4130_provenance.