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- NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_assertion type Assertion NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_head.
- NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_provenance.
- NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_assertion evidence source_evidence_curated NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_provenance.
- NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_assertion SIO_000772 19131948 NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_provenance.
- NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_assertion wasDerivedFrom uniprot-2016 NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_provenance.
- NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_assertion wasGeneratedBy ECO_0000218 NP5646.RAp-MJoTZbMftj2i-V3FXg388_vmMPU3UYuLVM5XtTUQQ130_provenance.