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- NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_assertion type Assertion NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_head.
- NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_assertion wasGeneratedBy ECO_0000203 NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_provenance.
- NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_assertion wasDerivedFrom befree-20150227 NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_provenance.
- NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_assertion SIO_000772 19878917 NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_provenance.
- NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_assertion evidence source_evidence_literature NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_provenance.
- NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559872.RAH1pTbdJj2ndrE1rDPKKCKa3xRgCAY6yPKbdtdoinbBM130_provenance.