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- source_evidence_literature type ECO_0000212 NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_assertion description "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_assertion evidence source_evidence_literature NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_assertion SIO_000772 11408949 NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_assertion wasDerivedFrom befree-20150227 NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_assertion wasGeneratedBy ECO_0000203 NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.