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- NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_assertion type Assertion NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_head.
- NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_assertion wasGeneratedBy ECO_0000203 NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_provenance.
- NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_assertion wasDerivedFrom befree-2016 NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_provenance.
- NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_assertion SIO_000772 15880323 NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_provenance.
- NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_assertion evidence source_evidence_literature NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_provenance.
- NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_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." NP493711.RAOlwsXJbk-OSExf_9AvczgnguJBl0alI2Dkg2koExlaE130_provenance.