Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_assertion> ?p ?o ?g. }
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- NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_assertion type Assertion NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_head.
- NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_assertion description "[Autosomal recessive Robinow syndrome (OMIM 268310) is a condition caused by mutations in the ROR2 gene, the receptor tyrosine kinase-like orphan receptor 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_provenance.
- NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_assertion evidence source_evidence_literature NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_provenance.
- NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_assertion SIO_000772 22178368 NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_provenance.
- NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_assertion wasDerivedFrom befree-2016 NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_provenance.
- NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_assertion wasGeneratedBy ECO_0000203 NP947447.RA0J8B2BK_7qTLAJZl7fCR_CSGlm6ZdZQJ3zsSLA5givU130_provenance.