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- source_evidence_literature type ECO_0000212 NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.
- befree-2016 importedOn "2016-02-19" NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.
- NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_assertion wasGeneratedBy ECO_0000203 NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.
- NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_assertion wasDerivedFrom befree-2016 NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.
- NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_assertion SIO_000772 15880323 NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.
- NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_assertion evidence source_evidence_literature NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.
- NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_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." NP493712.RA_h08dHz0Py87HPXsObvm8v9V9cateESxuoivxd8qC28130_provenance.