Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.
- NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_assertion description "[This review focuses on the eight monogenic primary dystonias, six of which are associated with an early-onset generalized phenotype (DYT1, 2, 4, 6, 16 and 17), while the remaining two are characterized by an adolescent- or adult-onset focal or segmental form of dystonia (DYT7 and 13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.
- NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_assertion evidence source_evidence_literature NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.
- NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_assertion SIO_000772 20590811 NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.
- NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_assertion wasDerivedFrom befree-2016 NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.
- NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_assertion wasGeneratedBy ECO_0000203 NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.
- befree-2016 importedOn "2016-02-19" NP822551.RAouh3z15KxZenIItnsTV1neBq4587ek0_RaNiDu86C10130_provenance.