Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.
- NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_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." NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.
- NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_assertion evidence source_evidence_literature NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.
- NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_assertion SIO_000772 23519333 NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.
- NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_assertion wasDerivedFrom befree-20140225 NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.
- NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_assertion wasGeneratedBy ECO_0000203 NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP865780.RAVCrN-Qr-yKnoe1xqHkPN8U3Oj9nkaX1Co2tEuWI-gSc130_provenance.