Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_assertion> ?p ?o ?g. }
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- NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_assertion type Assertion NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_head.
- NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_assertion description "[The abnormal phenotypes of the Hspg2-/- skeleton are similar to those of thanatophoric dysplasia (TD) type I, which is caused by activating mutations in FGFR3 (refs 7, 8, 9), and to those of Fgfr3 gain-of-function mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_provenance.
- NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_assertion evidence source_evidence_literature NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_provenance.
- NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_assertion SIO_000772 10545953 NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_provenance.
- NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_assertion wasDerivedFrom befree-2016 NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_provenance.
- NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_assertion wasGeneratedBy ECO_0000203 NP266749.RAUq_p-XbNt7M8n6VM_l6QXRRswD95bjMns11l3YnZJFA130_provenance.