Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.
- NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_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." NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.
- NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_assertion evidence source_evidence_literature NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.
- NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_assertion SIO_000772 18828673 NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.
- NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_assertion wasDerivedFrom befree-2016 NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.
- NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_assertion wasGeneratedBy ECO_0000203 NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP695793.RARggNHE5ovxmexUChWI8ah27xtcnNF0MEztHyeK8jjlQ130_provenance.