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- NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_assertion type Assertion NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_head.
- NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_assertion wasGeneratedBy ECO_0000203 NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_provenance.
- NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_assertion wasDerivedFrom befree-20150227 NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_provenance.
- NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_assertion SIO_000772 25064402 NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_provenance.
- NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_assertion evidence source_evidence_literature NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_provenance.
- NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_assertion description "[As rare abnormalities, we identified a submicroscopic deletion involving FGFR1 and an SOX3 polyalanine deletion in patients with IHH, and a WDR11 splice site mutation in a patient with CPHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400496.RA9ImwXzhZK_vGB52xSCCYvn8QYFnfZXyp_PSccwhGXlQ130_provenance.