Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP429776.RA2PMSMyLFZduDaqmWRo7Q-eKKCjXhE5pTPnk0HWWRTOU130_provenance.