Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.
- NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_assertion description "[The clinical presentations of patients with mutations in TH and SPR genes were strikingly more complex, characterized by mental retardation, oculogyric crises and parkinsonism and they were all classified as Dopa-responsive dystonia-plus syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.
- NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_assertion evidence source_evidence_literature NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.
- NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_assertion SIO_000772 19491146 NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.
- NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_assertion wasDerivedFrom befree-20140225 NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.
- NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_assertion wasGeneratedBy ECO_0000203 NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP474020.RAGwkMgYqOzELWMvnnaPudfHESaSfIKJc4D5g5umudJt0130_provenance.