Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_assertion> ?p ?o ?g. }
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- NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_assertion type Assertion NP588.RAtNw_NwnNuJR_dGYlCkYhtVVBO-Jf4M11tmU0tREKtto130_head.
- 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.