Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.
- NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_assertion description "[In this study, we screened the ARX gene in 226 male patients with autism spectrum disorders and mental retardation; 42 of the patients had epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.
- NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_assertion evidence source_evidence_literature NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.
- NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_assertion SIO_000772 17044103 NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.
- NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_assertion wasDerivedFrom befree-20150227 NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.
- NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_assertion wasGeneratedBy ECO_0000203 NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978192.RAe0KcrH4J8P5kVI89m1KoMgmlVBhcvgG2Su-KCIOSFh8130_provenance.