Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_assertion> ?p ?o ?g. }
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- NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_assertion type Assertion NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_head.
- NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_assertion description "[Dyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant pigmentary genodermatosis characterized by hyperpigmented and hypopigmented macules of on the extremities and caused by the mutations in the ADAR gene(also called DSRAD) encoding for RNA-specific adenosine deaminase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_provenance.
- NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_assertion evidence source_evidence_literature NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_provenance.
- NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_assertion SIO_000772 15146470 NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_provenance.
- NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_assertion wasDerivedFrom befree-20150227 NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_provenance.
- NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_assertion wasGeneratedBy ECO_0000203 NP223025.RAsUH_FpiiTPPJK_bL2TPKBYL2GS0c-g55nswpwM2TdIk130_provenance.