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- source_evidence_literature type ECO_0000212 NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.
- NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_assertion description "[Independently, we also identified compound heterozygous WDR19 mutations by exome sequencing in a Moroccan family with isolated nephronophthisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.
- NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_assertion evidence source_evidence_literature NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.
- NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_assertion SIO_000772 22019273 NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.
- NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_assertion wasDerivedFrom befree-2016 NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.
- NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_assertion wasGeneratedBy ECO_0000203 NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.
- befree-2016 importedOn "2016-02-19" NP932808.RA9Cf8zjOmSVJFNUAn7Htk5nz1fpfJPf4y_rGinkUC-xc130_provenance.