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- NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_assertion type Assertion NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_head.
- NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_assertion description "[Congenital nephrotic syndrome of the Finnish type (NPHS1, CNF) is an autosomal recessively inherited disease occurring due to mutations in the nephrin gene (NPHS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_provenance.
- NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_assertion evidence source_evidence_literature NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_provenance.
- NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_assertion SIO_000772 16362719 NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_provenance.
- NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_assertion wasDerivedFrom befree-20150227 NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_provenance.
- NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_assertion wasGeneratedBy ECO_0000203 NP597375.RAZBtQdsjcDb5HeHq2XkaYVaQJCIaq2YjLF9L8Ys_o-Gg130_provenance.