Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.
- NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_assertion description "[Such conditions include Wilson's disease, Hallervorden-Spatz disease (HSD), juvenile form of Huntington's disease, juvenile neuronal ceroid lipofuscinosis, early-onset Machado-Joseph disease neuroacanthocytosis, storage disorders, and variant form of dopa-response dystonias (DRD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.
- NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_assertion evidence source_evidence_literature NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.
- NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_assertion SIO_000772 14580665 NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.
- NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_assertion wasDerivedFrom befree-20140225 NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.
- NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_assertion wasGeneratedBy ECO_0000203 NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP790084.RA_CfhaoJaRUGJMaaseExnAvzn80UawPI7myb2fp-kWSo130_provenance.