Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.
- NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_assertion description "[Given the overlap of this autism/mental retardation (MR) phenotype and the MR-associated disorders in our patients, together with the fact that mapping of the additional autosomal breakpoints involved did not disclose obvious candidate disease genes, we ascertain with this study that AUTS2 mutations are clearly linked to autosomal dominant mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.
- NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_assertion evidence source_evidence_literature NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.
- NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_assertion SIO_000772 17211639 NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.
- NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_assertion wasDerivedFrom befree-2016 NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.
- NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_assertion wasGeneratedBy ECO_0000203 NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.
- befree-2016 importedOn "2016-02-19" NP587917.RA6Cw2BsFnNbNod79v6ur3UYjdwaaOgTSr4XSljdB1SNg130_provenance.