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- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion type Assertion NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_head.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion description "[MYH9-associated disorders (May-Hegglin anomaly, Epstein and Fechtner syndrome, and others) are inherited in an autosomal dominant manner and characterized by defects in different organs (including eyes, ears, kidneys and thrombocytes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion evidence source_evidence_literature NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion SIO_000772 23144074 NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion wasDerivedFrom befree-20140225 NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion wasGeneratedBy ECO_0000203 NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.