Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.
- NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_assertion wasGeneratedBy ECO_0000203 NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.
- NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_assertion wasDerivedFrom befree-20150227 NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.
- NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_assertion SIO_000772 20531469 NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.
- NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_assertion evidence source_evidence_literature NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.
- NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_assertion description "[When comparing 996 ASD individuals of European ancestry to 1,287 matched controls, cases were found to carry a higher global burden of rare, genic copy number variants (CNVs) (1.19 fold, P = 0.012), especially so for loci previously implicated in either ASD and/or intellectual disability (1.69 fold, P = 3.4 x 10(-4)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253436.RApRoJTOBNP0vM20rNNcg0S7bMtWRYVgJ32xnXng7kdJ8130_provenance.