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- NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_assertion type Assertion NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_head.
- NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_assertion wasGeneratedBy ECO_0000203 NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_provenance.
- NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_assertion wasDerivedFrom befree-20150227 NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_provenance.
- NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_assertion SIO_000772 12414817 NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_provenance.
- NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_assertion evidence source_evidence_literature NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_provenance.
- NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_assertion description "[Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898143.RAbtB0valsJCtmzLXHcOLy1drraoKe_nxE3PDB-kOphEo130_provenance.