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- source_evidence_literature type ECO_0000212 NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.
- NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_assertion description "[We characterized the genomic organization of human PCDH21 and performed mutation screening in 224 patients with autosomal recessive retinitis pigmentosa, 29 patients with Leber congenital amaurosis, and 26 patients with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.
- NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_assertion evidence source_evidence_literature NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.
- NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_assertion SIO_000772 16288196 NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.
- NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_assertion wasDerivedFrom gad-20150221 NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.
- NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_assertion wasGeneratedBy ECO_0000203 NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP97175.RAo7o5ECo7jZU_9vbCAjYYpOsB4H11Dp6SKaYEigqsHsM130_provenance.