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- source_evidence_literature type ECO_0000212 NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.
- NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_assertion wasGeneratedBy ECO_0000203 NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.
- NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_assertion wasDerivedFrom befree-20150227 NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.
- NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_assertion SIO_000772 15880323 NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.
- NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_assertion evidence source_evidence_literature NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.
- NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_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." NP319869.RAcVyVcEc7Gp91xzkZixbHa2lUj7Ts_QcH7plJH6YVx3o130_provenance.