Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_assertion description "[DYT16 dystonia is a novel recessive form of EO-PD, recently described in few patients, caused by mutations in the PRKRA gene located at chromosome 2q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_assertion evidence source_evidence_literature NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_assertion SIO_000772 19157930 NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_assertion wasDerivedFrom befree-20150227 NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_assertion wasGeneratedBy ECO_0000203 NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP798784.RABpGndj9wBVKs8EkEJrVWbwIXWZqmIIoy2JN1CFAEWpQ130_provenance.