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- source_evidence_literature type ECO_0000212 NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.
- NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_assertion description "[Mutations in the homologous human peripherin/RDS gene can cause autosomal dominant retinitis pigmentosa, but these are missense mutations or deletions of single codons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.
- NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_assertion evidence source_evidence_literature NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.
- NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_assertion SIO_000772 8485575 NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.
- NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_assertion wasDerivedFrom befree-2016 NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.
- NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_assertion wasGeneratedBy ECO_0000203 NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1343021.RAr0PKDxRq6xQrWLCytl-_O5nJdDnOo8WPMyYnU_Z-4AQ130_provenance.