Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.
- NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_assertion description "[Rapid-onset dystonia-parkinsonism (RDP) (also known as DYT12) is characterized by the abrupt onset of dystonia and parkinsonism and is caused by mutations in the ATP1A3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.
- NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_assertion evidence source_evidence_literature NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.
- NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_assertion SIO_000772 17282997 NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.
- NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_assertion wasDerivedFrom befree-2016 NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.
- NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_assertion wasGeneratedBy ECO_0000203 NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.
- befree-2016 importedOn "2016-02-19" NP592425.RAGh0ntmMyTpKonTbf4eC7sqpf_Jee4f6vxmMRq9J0pGE130_provenance.