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- NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_assertion type Assertion NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_head.
- NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_assertion wasGeneratedBy ECO_0000203 NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_provenance.
- NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_assertion wasDerivedFrom befree-20140225 NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_provenance.
- NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_assertion SIO_000772 18853461 NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_provenance.
- NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_assertion evidence source_evidence_literature NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_provenance.
- NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_assertion description "[Arthrogryposis, Renal dysfunction and Cholestasis (ARC) syndrome is a multi-system autosomal recessive disorder caused by germline mutations in VPS33B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765508.RApS37UUZFmyf0coLK1qNYhiP93Iief8eavnzn1365_lU130_provenance.