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- source_evidence_literature type ECO_0000212 NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.
- befree-2016 importedOn "2016-02-19" NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.
- NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_assertion wasGeneratedBy ECO_0000203 NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.
- NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_assertion wasDerivedFrom befree-2016 NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.
- NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_assertion SIO_000772 15880323 NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.
- NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_assertion evidence source_evidence_literature NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.
- NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_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." NP493714.RAM7vFCF0bcNsbFR529Wyd1qp9BI532iY_fqru3ziJELI130_provenance.