Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_assertion type Assertion NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_head.
- NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_assertion description "[Mutations in the type II collagen gene account for most spondyloepiphyseal dysplasia and spondyloepiphyseal dysplasia-like clinical disorders, whereas mutations in the fibroblast growth factor receptor 3 gene are responsible for achondroplasia, thanatophoric dysplasia, and hypochondroplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_provenance.
- NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_assertion evidence source_evidence_literature NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_provenance.
- NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_assertion SIO_000772 8879993 NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_provenance.
- NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_assertion wasDerivedFrom befree-20150227 NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_provenance.
- NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_assertion wasGeneratedBy ECO_0000203 NP401298.RAVzLXYYFzUwoOgoVwV3dtxdN1f9hDk_FqSjdpWW1qmaU130_provenance.