Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_assertion> ?p ?o ?g. }
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- NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_assertion type Assertion NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_head.
- NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_assertion description "[A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_provenance.
- NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_assertion evidence source_evidence_curated NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_provenance.
- NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_assertion SIO_000772 23636107 NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_provenance.
- NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_assertion wasDerivedFrom uniprot-2016 NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_provenance.
- NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_assertion wasGeneratedBy ECO_0000218 NP7471.RAdOc9zc8t9y_hBpEtmw_hk86Z2lwvqeKklgORyEjqmdM130_provenance.