Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.
- NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_assertion description "[It is necessary to distinguish between lethal mutations leading to diseases such as MCAD and LQTS, and polymorphisms (for instance, in the IL-10 gene and mtDNA) that are normal gene variants but might be suboptimal in critical situations and thus predispose infants to sudden infant death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.
- NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_assertion evidence source_evidence_literature NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.
- NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_assertion SIO_000772 15466077 NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.
- NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_assertion wasDerivedFrom befree-20140225 NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.
- NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_assertion wasGeneratedBy ECO_0000203 NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP389518.RA61l04DfQZB_aNQalqMdsK2zB4v00MLQjpjKqKyyy9Qc130_provenance.