Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.
- NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_assertion description "[We have screened the CDKL5 gene in 94 patients with RTT or a RTT-like phenotype who had tested negative for MECP2 mutations (13 classical RTT female subjects, 25 atypical RTT female subjects, 40 RTT-like female and 16 RTT-like male subjects; 33 of the patients had early onset seizures).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.
- NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_assertion evidence source_evidence_literature NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.
- NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_assertion SIO_000772 16015284 NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.
- NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_assertion wasDerivedFrom befree-2016 NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.
- NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_assertion wasGeneratedBy ECO_0000203 NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.
- befree-2016 importedOn "2016-02-19" NP503962.RAst6FRJQHk2eWzXITajC8D2xTSrasFK0p-a4ikUl1Qto130_provenance.