Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_assertion wasGeneratedBy ECO_0000203 NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_assertion wasDerivedFrom befree-2016 NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_assertion SIO_000772 17187067 NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_assertion evidence source_evidence_literature NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_assertion description "[NLSDM is distinct from Chanarin-Dorfman syndrome, which is characterized by neutral lipid storage disease with ichthyosis, mild myopathy and hepatomegaly due to mutations in ABHD5 (also known as CGI-58).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.