Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_assertion> ?p ?o ?g. }
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- NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_assertion type Assertion NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_head.
- NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_assertion description "[The commonest genetic form of juvenile or early adult onset macular degeneration is Stargardt Disease (STGD) caused by recessive mutations in the gene ABCA4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_provenance.
- NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_assertion evidence source_evidence_literature NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_provenance.
- NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_assertion SIO_000772 22863181 NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_provenance.
- NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_assertion wasDerivedFrom befree-2016 NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_provenance.
- NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_assertion wasGeneratedBy ECO_0000203 NP1002718.RAPXfw1a2-IK0X1UKVB7L2ojPrgUAgAc5oIJpGKV0fDNo130_provenance.