Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.
- NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_assertion description "[In this study we used 1 Mb genome-wide array-CGH to screen 48 children with MR and congenital malformations for submicroscopic chromosomal imbalances, where the underlying cause was unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.
- NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_assertion evidence source_evidence_literature NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.
- NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_assertion SIO_000772 17901693 NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.
- NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_assertion wasDerivedFrom befree-20140225 NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.
- NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_assertion wasGeneratedBy ECO_0000203 NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP253068.RAeL1wJRBTzXFwq-jLTy0sdFwKjkFQgKuRaPOQVNHfbEQ130_provenance.