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- NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_assertion type Assertion NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_head.
- NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_assertion wasGeneratedBy ECO_0000203 NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_provenance.
- NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_assertion wasDerivedFrom befree-20150227 NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_provenance.
- NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_assertion SIO_000772 23142271 NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_provenance.
- NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_assertion evidence source_evidence_literature NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_provenance.
- NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_assertion description "[The finding of known loss of function variants in ciliopathy associated genes, AHI1, BBS2 and BBS4 in addition to KIF7 mutations provides evidence for oligogenic inheritance in ACLS and suggests that this might contribute to the phenotypic variability of KIF7-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988650.RAK3ETnjau3pqaoguJYLCZc35OC8rdImLX2pcJntZ04XE130_provenance.