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- source_evidence_literature type ECO_0000212 NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.
- NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_assertion description "[One of the genes that causes albinism encodes for an orphan GPCR (OA1) expressed only in pigmented cells, including the RPE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.
- NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_assertion evidence source_evidence_literature NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.
- NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_assertion SIO_000772 18828673 NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.
- NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_assertion wasDerivedFrom befree-2016 NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.
- NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_assertion wasGeneratedBy ECO_0000203 NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.
- befree-2016 importedOn "2016-02-19" NP695791.RAmU3bolO1J2ovqsDIpNaK0zOWjuJdf0SAaFpKzoB7R9k130_provenance.