Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.
- NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_assertion description "[X-linked cyclin-dependent kinase-like 5 (CDKL5 or STK9) has recently been implicated in atypical Rett and X-linked West syndromes, severe neurological disorders associated with mental retardation, loss of communication and motor skills and infantile spasms and seizures in predominantly females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.
- NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_assertion evidence source_evidence_literature NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.
- NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_assertion SIO_000772 16330482 NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.
- NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_assertion wasDerivedFrom befree-20140225 NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.
- NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_assertion wasGeneratedBy ECO_0000203 NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP813918.RA_46Y-nMWhGjrKs-0RhSLUjgAVngvJPygiRozgI1UD4o130_provenance.