Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_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." NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_assertion evidence source_evidence_literature NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_assertion SIO_000772 24534191 NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_assertion wasDerivedFrom befree-20150227 NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_assertion wasGeneratedBy ECO_0000203 NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.