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- NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_assertion type Assertion NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_head.
- NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_assertion description "[We confirm an overlap in the NPHS1/NPHS2 mutation spectrum with the characterization of a unique di-genic inheritance of NPHS1 and NPHS2 mutations, which results in a 'tri-allelic' hit and appears to modify the phenotype from CNF to one of congenital focal segmental glomerulosclerosis (FSGS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_provenance.
- NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_assertion evidence source_evidence_literature NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_provenance.
- NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_assertion SIO_000772 11854170 NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_provenance.
- NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_assertion wasDerivedFrom befree-2016 NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_provenance.
- NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_assertion wasGeneratedBy ECO_0000203 NP345682.RAEWovesHNW30QIs9T8VFk_inpRIg4nAPi3VxfOgFVeig130_provenance.