Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.
- NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_assertion description "[We progressively screened DNA samples from 613 individuals with ID initially for the most frequent ARX mutations (c.304ins(GCG)(7)'expansion' of pA1 and c.429_452dup 'dup24bp' of pA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.
- NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_assertion evidence source_evidence_literature NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.
- NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_assertion SIO_000772 21496008 NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.
- NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_assertion wasDerivedFrom befree-20140225 NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.
- NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_assertion wasGeneratedBy ECO_0000203 NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP236727.RAFypG3mZBET2Whajmdxa2K8bPJC5rde6ANi04M_9XpTI130_provenance.