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- NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_assertion type Assertion NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_head.
- NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_assertion wasGeneratedBy ECO_0000203 NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_provenance.
- NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_assertion wasDerivedFrom befree-20140225 NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_provenance.
- NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_assertion SIO_000772 22039234 NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_provenance.
- NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_assertion evidence source_evidence_literature NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_provenance.
- NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_assertion description "[Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371747.RAQUh2Yd_gP65IzaX4XBgeyyP4_7CqaK9yh5KNJcp2HsI130_provenance.