Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_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." NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion evidence source_evidence_literature NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion SIO_000772 19131948 NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion wasDerivedFrom gad-20150221 NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_assertion wasGeneratedBy ECO_0000203 NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP137882.RAbPuSridZypbTEDsnSq9kNOCCoT4fy1ky4oFIOndGrTY130_provenance.