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- NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_assertion type Assertion NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_head.
- NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_assertion description "[Cohen syndrome (CS) is a rare autosomal recessive condition caused by mutations and/or large rearrangements in the VPS13B gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_provenance.
- NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_assertion evidence source_evidence_literature NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_provenance.
- NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_assertion SIO_000772 23188044 NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_provenance.
- NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_assertion wasDerivedFrom befree-2016 NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_provenance.
- NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_assertion wasGeneratedBy ECO_0000203 NP1031805.RAJNzoidfjx9xaLIGV4k1VAuM53Ptzxbg_FLFTaxib3NI130_provenance.