Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.
- NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_assertion description "[In the remaining 5 individuals with PCD who underwent exome sequencing, we identified mutations in two genes (DNAI2, DNAH5) known to cause PCD, including an Ashkenazi Jewish founder mutation in DNAI2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.
- NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_assertion evidence source_evidence_literature NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.
- NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_assertion SIO_000772 23261302 NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.
- NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_assertion wasDerivedFrom befree-20140225 NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.
- NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_assertion wasGeneratedBy ECO_0000203 NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP918325.RAGLwt4OgNKfBFYUcn46lQrzLKYlYgxpUc2LGXBxho_Zk130_provenance.