Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.
- NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_assertion description "[The complete clinical phenotype of dup(7)(p15-->pter) includes mental retardation, skull anomalies, large anterior fontanel, cardiovascular defects, joint dislocation and contraction, and gastrointestinal and genital defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.
- NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_assertion evidence source_evidence_literature NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.
- NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_assertion SIO_000772 8741912 NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.
- NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_assertion wasDerivedFrom befree-20140225 NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.
- NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_assertion wasGeneratedBy ECO_0000203 NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625611.RACyUhFa1n4riVhRXlon9no904Euqywp8RHuIs4Yd9fRE130_provenance.