Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.
- NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_assertion wasGeneratedBy ECO_0000203 NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.
- NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_assertion wasDerivedFrom befree-20140225 NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.
- NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_assertion SIO_000772 10408773 NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.
- NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_assertion evidence source_evidence_literature NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.
- NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_assertion description "[The Hallopeau-Siemens variant of recessive dystrophic epidermolysis bullosa (HS-RDEB) is a severe inherited skin disease characterized by the absence of collagen type VII (COLVII) and anchoring fibrils (AF), caused by mutations in collagen type VII gene (COL7A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.
- befree-20140225 importedOn "2014-02-25" NP347991.RAOYs_RO5soJBDWmZw8LmXQfUfvRfW5mZOpKuMAx-g894130_provenance.