Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_assertion> ?p ?o ?g. }
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- NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_assertion type Assertion NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_head.
- NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_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." NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.
- NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_assertion evidence source_evidence_literature NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.
- NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_assertion SIO_000772 19131948 NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.
- NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_assertion wasDerivedFrom befree-20140225 NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.
- NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_assertion wasGeneratedBy ECO_0000203 NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.