Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.
- NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_assertion wasGeneratedBy ECO_0000218 NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.
- NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_assertion wasDerivedFrom uniprot-2016 NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.
- NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_assertion SIO_000772 9767294 NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.
- NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_assertion evidence source_evidence_curated NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.
- NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_assertion description "[Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9903.RANaJiZmGaxu1fUyzO8J6R_t-e5T82D3hFrK4Kr5UFddY130_provenance.