Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_assertion description "[Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_assertion evidence source_evidence_literature NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_assertion SIO_000772 17273969 NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_assertion wasDerivedFrom befree-2016 NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_assertion wasGeneratedBy ECO_0000203 NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- befree-2016 importedOn "2016-02-19" NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.