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- NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_assertion type Assertion NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_head.
- NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_provenance.
- NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_assertion evidence source_evidence_literature NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_provenance.
- NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_assertion SIO_000772 1610568 NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_provenance.
- NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_assertion wasDerivedFrom befree-20140225 NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_provenance.
- NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_assertion wasGeneratedBy ECO_0000203 NP824790.RAGKFyJhQ91fsZMYvr13vfWwkzkC7rOIWkx_k03B1Ivow130_provenance.