Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.
- NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_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." NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.
- NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_assertion evidence source_evidence_literature NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.
- NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_assertion SIO_000772 15466077 NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.
- NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_assertion wasDerivedFrom befree-20150227 NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.
- NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_assertion wasGeneratedBy ECO_0000203 NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP503756.RAWsF9Q3TQVwMCxJXorgfBLzEQ-BZr-uUms3XM99Yr7fg130_provenance.