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- NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_assertion type Assertion NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_head.
- NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_assertion description "[OMD is clinically and genetically heterogeneous, with different morphologic features and progression in outer retinal pathology according to RP1L1 gene mutations, indicating the genotype-phenotype correlation in patients with OMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_provenance.
- NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_assertion evidence source_evidence_literature NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_provenance.
- NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_assertion SIO_000772 23745001 NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_provenance.
- NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_assertion wasDerivedFrom befree-20150227 NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_provenance.
- NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_assertion wasGeneratedBy ECO_0000203 NP963176.RARRHWDbrljDHPjsN1cPQEUDxGwHfNJB2INlwtgRY8-Po130_provenance.