Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.
- NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_assertion description "[Dyschromatosis universalis hereditaria (DUH) is a pigmentary genodermatosis characterized by a mixture of hyperpigmented and hypopigmented macules distributed randomly over the body.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.
- NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_assertion evidence source_evidence_literature NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.
- NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_assertion SIO_000772 23519333 NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.
- NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_assertion wasDerivedFrom befree-2016 NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.
- NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_assertion wasGeneratedBy ECO_0000203 NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1062502.RA3Rl8e-13zyWdRpKCsDkvR_bnpG9I8HtGMYkxjinB3iE130_provenance.