Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_assertion> ?p ?o ?g. }
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- NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_assertion type Assertion NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_head.
- NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_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." NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_provenance.
- NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_assertion evidence source_evidence_literature NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_provenance.
- NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_assertion SIO_000772 19131948 NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_provenance.
- NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_assertion wasDerivedFrom befree-2016 NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_provenance.
- NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_assertion wasGeneratedBy ECO_0000203 NP713081.RAbACVJH1fdX-bsQSooVqpBe8uEC0XmEVAS4YpdOAuEaE130_provenance.