Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.
- NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_assertion description "[The strategy was designed to suppress both the mutated and the wild-type hRHO allele in a mutational-independent fashion, to overcome mutational heterogeneity of autosomal dominant retinitis pigmentosa due to hRHO mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.
- NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_assertion evidence source_evidence_literature NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.
- NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_assertion SIO_000772 21268285 NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.
- NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_assertion wasDerivedFrom befree-20140225 NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.
- NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_assertion wasGeneratedBy ECO_0000203 NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP219471.RAVQu1q8Dkqril-3D8f-ND57UIK0W-ErBgcxbantd7CX8130_provenance.