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- NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_assertion type Assertion NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_head.
- NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_assertion wasGeneratedBy ECO_0000203 NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_provenance.
- NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_assertion wasDerivedFrom befree-2016 NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_provenance.
- NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_assertion SIO_000772 15880323 NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_provenance.
- NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_assertion evidence source_evidence_literature NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_provenance.
- NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_assertion description "[It is unclear whether individuals with TBMN and impaired renal function represent part of the spectrum of TBMN associated with heterozygous COL4A3 or COL4A4 mutations, or if their disease is caused by mutations of other genes, or whether it is caused by a second coexistent renal lesion or is misdiagnosed Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493713.RA34dFAMgmvK_Ok_8kFX3P7sl2pf7ddKeXe5cxrehEn6M130_provenance.