Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_assertion description "[DYT1 dystonia is caused by an autosomal dominant mutation that leads to a glutamic acid deletion in torsinA (TA), a member of the AAA+ ATPase superfamily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_assertion evidence source_evidence_literature NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_assertion SIO_000772 21102408 NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_assertion wasDerivedFrom befree-2016 NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_assertion wasGeneratedBy ECO_0000203 NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.
- befree-2016 importedOn "2016-02-19" NP854121.RAGx18TtLvKkHIDUY1Lar7CjAEiAvVaGvVYLYHX13lvCo130_provenance.