Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_assertion> ?p ?o ?g. }
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- NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_assertion type Assertion NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_head.
- NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_provenance.
- NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_assertion evidence source_evidence_literature NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_provenance.
- NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_assertion SIO_000772 23063620 NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_provenance.
- NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_assertion wasDerivedFrom befree-2016 NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_provenance.
- NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_assertion wasGeneratedBy ECO_0000203 NP1020657.RAvh6Y6yXgcR1iPXvqHtVxw-73wR9IqO2612X6rqtxmPI130_provenance.