Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_assertion> ?p ?o ?g. }
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- NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_assertion type Assertion NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_head.
- NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_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." NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_provenance.
- NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_assertion evidence source_evidence_literature NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_provenance.
- NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_assertion SIO_000772 19131948 NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_provenance.
- NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_assertion wasDerivedFrom gad-20150221 NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_provenance.
- NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_assertion wasGeneratedBy ECO_0000203 NP118784.RABFnnaWX1Nzm8l_r1GLivBeIVQv27eo6UTwc7U4c4VUk130_provenance.