Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_assertion wasGeneratedBy ECO_0000203 NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_assertion wasDerivedFrom lhgdn-20090331 NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_assertion SIO_000772 15492925 NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_assertion evidence source_evidence_literature NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.