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- NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_assertion type Assertion NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_head.
- NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_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." NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_provenance.
- NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_assertion evidence source_evidence_literature NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_provenance.
- NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_assertion SIO_000772 16362719 NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_provenance.
- NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_assertion wasDerivedFrom befree-20140225 NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_provenance.
- NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_assertion wasGeneratedBy ECO_0000203 NP724394.RARLPKyZTRapYSL46WEP2QZSSWzxffJ0zE-w_vFv_8OnE130_provenance.