Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_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." NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_assertion evidence source_evidence_literature NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_assertion SIO_000772 24534191 NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_assertion wasDerivedFrom befree-20150227 NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_assertion wasGeneratedBy ECO_0000203 NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.