Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.
- NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_assertion wasGeneratedBy ECO_0000203 NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.
- NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_assertion wasDerivedFrom befree-20140225 NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.
- NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_assertion SIO_000772 10597140 NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.
- NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_assertion evidence source_evidence_literature NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.
- NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_assertion description "[Epidermolytic hyperkeratosis (EHK) is a genodermatosis caused by mutations in either the keratin 1 (K1) or keratin 10 (K10) genes, and characterized by erythroderma and blistering at birth, with development of a ribbed, ichthyotic hyperkeratosis and palmoplantar keratoderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP511299.RAsiBhZSAURX8Ji9k3zT302_klCQ6Ef5E3ic_g9rWQxHI130_provenance.