Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_assertion evidence source_evidence_literature NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_assertion SIO_000772 24534191 NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_assertion wasDerivedFrom befree-2016 NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_assertion wasGeneratedBy ECO_0000203 NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.