Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.
- NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_assertion description "[The results of this study showed that the vast majority of all individuals with 22q11 deletion syndrome have behavior and/or learning problems and more than 40% meet criteria for either ASD, ADHD or both.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.
- NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_assertion evidence source_evidence_literature NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.
- NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_assertion SIO_000772 19070990 NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.
- NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_assertion wasDerivedFrom befree-20150227 NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.
- NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_assertion wasGeneratedBy ECO_0000203 NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP253432.RA8-zv1n3FobwDOWm8Kn6Wwb0hwCAhx7956Cid1sOeumA130_provenance.