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- NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_assertion type Assertion NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_head.
- NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_provenance.
- NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_assertion evidence source_evidence_literature NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_provenance.
- NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_assertion SIO_000772 21858451 NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_provenance.
- NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_assertion wasDerivedFrom befree-20140225 NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_provenance.
- NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_assertion wasGeneratedBy ECO_0000203 NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_provenance.