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- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion type Assertion NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_head.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_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." NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion evidence source_evidence_literature NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion SIO_000772 19131948 NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion wasDerivedFrom gad-20150221 NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion wasGeneratedBy ECO_0000203 NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.