Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
- NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_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." NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
- NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_assertion evidence source_evidence_curated NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
- NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_assertion SIO_000772 19131948 NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
- NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_assertion wasDerivedFrom uniprot-20130724 NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
- NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_assertion wasGeneratedBy ECO_0000218 NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP352.RAIWuGP7gaJPCuA6eLVytqaaNz37E3FfFtR3bSLsr5Hwc130_provenance.