Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.
- NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_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." NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.
- NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_assertion evidence source_evidence_literature NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.
- NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_assertion SIO_000772 19491146 NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.
- NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_assertion wasDerivedFrom befree-20140225 NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.
- NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_assertion wasGeneratedBy ECO_0000203 NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP865107.RA7NOarwq4rsNb0PX6NaldKn4m_Py97V8ulhlbVaev7Jg130_provenance.