Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.
- NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_assertion description "[The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.
- NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_assertion evidence source_evidence_literature NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.
- NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_assertion SIO_000772 7922453 NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.
- NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_assertion wasDerivedFrom befree-20140225 NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.
- NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_assertion wasGeneratedBy ECO_0000203 NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223782.RABqB3Vys3iih1x-W9HXnHPBAgo1_SB0ThPbEF8aFlfZs130_provenance.