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- NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_assertion type Assertion NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_head.
- NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_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." NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_provenance.
- NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_assertion evidence source_evidence_literature NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_provenance.
- NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_assertion SIO_000772 19131948 NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_provenance.
- NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_assertion wasDerivedFrom gad-20150221 NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_provenance.
- NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_assertion wasGeneratedBy ECO_0000203 NP137881.RAPE0xw4pTVCqVD03ccSbYXeob_vmEsE-CXGhKYVWndlQ130_provenance.