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- NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_assertion type Assertion NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_head.
- NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_assertion wasGeneratedBy ECO_0000203 NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_provenance.
- NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_assertion wasDerivedFrom befree-2016 NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_provenance.
- NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_assertion SIO_000772 17216245 NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_provenance.
- NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_assertion evidence source_evidence_literature NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_provenance.
- NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588237.RA6ut48su7-RSqPWBbfICSBYfRUKZA29WhViqzPn0OC_g130_provenance.