Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_assertion> ?p ?o ?g. }
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- NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_assertion type Assertion NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_head.
- NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_assertion description "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_provenance.
- NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_assertion evidence source_evidence_literature NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_provenance.
- NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_assertion SIO_000772 12011143 NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_provenance.
- NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_assertion wasDerivedFrom befree-20150227 NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_provenance.
- NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_assertion wasGeneratedBy ECO_0000203 NP674192.RAS9Zp_FiOz44u5kJGOkA241MoETrlWNsOAcD8MSDmDqk130_provenance.