Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_assertion> ?p ?o ?g. }
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- NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_assertion type Assertion NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_head.
- NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_assertion description "[Other mutations within the FGFR3 tyrosine kinase domain (e.g., C1620A or C1620G [both resulting in Asn540Lys]) are known to cause hypochondroplasia, a relatively common but milder skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_provenance.
- NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_assertion evidence source_evidence_literature NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_provenance.
- NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_assertion SIO_000772 11055896 NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_provenance.
- NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_assertion wasDerivedFrom befree-20140225 NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_provenance.
- NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_assertion wasGeneratedBy ECO_0000203 NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_provenance.