Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_assertion> ?p ?o ?g. }
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- NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_assertion type Assertion NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_head.
- NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_assertion description "[MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_provenance.
- NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_assertion evidence source_evidence_literature NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_provenance.
- NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_assertion SIO_000772 17427193 NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_provenance.
- NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_assertion wasDerivedFrom gad-20130706 NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_provenance.
- NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_assertion wasGeneratedBy ECO_0000203 NP67467.RAfheNY9zGTFNVCD_rPU0Vnclvb0-Z89YMu_UhvV9VYpQ130_provenance.