Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_assertion> ?p ?o ?g. }
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- NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_assertion type Assertion NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_head.
- NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_assertion description "[A new arginine substitution mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_provenance.
- NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_assertion evidence source_evidence_literature NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_provenance.
- NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_assertion SIO_000772 15659327 NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_provenance.
- NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_assertion wasDerivedFrom befree-2016 NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_provenance.
- NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_assertion wasGeneratedBy ECO_0000203 NP476916.RAZ6T49wWaz573eCLtZCw2ZEW8PmGn3Le9fg_axVDDw_g130_provenance.