Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.
- NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_assertion description "[Our results support the recent identification of mutations in ECEL1 as a disease gene in DA5D and expand the clinical and allelic spectrum of this condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.
- NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_assertion evidence source_evidence_curated NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.
- NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_assertion SIO_000772 23829171 NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.
- NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_assertion wasDerivedFrom uniprot-20150221 NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.
- NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_assertion wasGeneratedBy ECO_0000218 NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_provenance.