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- NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_assertion type Assertion NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_head.
- NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_assertion description "[Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_provenance.
- NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_assertion evidence source_evidence_literature NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_provenance.
- NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_assertion SIO_000772 10900517 NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_provenance.
- NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_assertion wasDerivedFrom befree-20150227 NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_provenance.
- NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_assertion wasGeneratedBy ECO_0000203 NP277441.RABKpyik3e3rmui-HwpN6KF-Rg9EPVSJtKodnbb_jv_wg130_provenance.