Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.
- NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_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." NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.
- NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_assertion evidence source_evidence_literature NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.
- NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_assertion SIO_000772 16330482 NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.
- NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_assertion wasDerivedFrom befree-2016 NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.
- NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_assertion wasGeneratedBy ECO_0000203 NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP525577.RAn2dxPGcDq0IVPDXyh4FlR2aIZusn09c00arysa1kykQ130_provenance.