Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_assertion> ?p ?o ?g. }
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- NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_assertion type Assertion NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_head.
- NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_assertion wasGeneratedBy ECO_0000203 NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_provenance.
- NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_assertion wasDerivedFrom befree-20150227 NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_provenance.
- NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_assertion SIO_000772 24392928 NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_provenance.
- NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_assertion evidence source_evidence_literature NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_provenance.
- NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_assertion description "[The aim of this study was to determine the frequency of mutations in tubulin genes (TUBB2B, TUBA1A, and TUBB3) in patients with malformations of cortical development (MCDs) of unknown origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841762.RApiAw6OLqnMHIjpwfx8TeYWyId9-HUwl2Q5w87893WMc130_provenance.