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- NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_assertion type Assertion NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_head.
- NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_assertion description "[RP is a retinal degeneration disorder that is caused by mutations of various genes, including semaphorin-4A (SEMA4A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_provenance.
- NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_assertion evidence source_evidence_literature NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_provenance.
- NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_assertion SIO_000772 22956603 NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_provenance.
- NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_assertion wasDerivedFrom befree-2016 NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_provenance.
- NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_assertion wasGeneratedBy ECO_0000203 NP1011007.RA3aInW6SY92BurSmgU7rviG8ySw7cgSkUCbWX7lGrkBI130_provenance.