Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.
- NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_assertion description "[Here, we studied variations in the exons and introns of the FMO3 gene by direct sequencing analysis and minisequencing in 159 SIDS cases and 170 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.
- NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_assertion evidence source_evidence_literature NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.
- NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_assertion SIO_000772 20198379 NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.
- NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_assertion wasDerivedFrom gad-20130706 NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.
- NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_assertion wasGeneratedBy ECO_0000203 NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87654.RAWfT6Zv6OWiQkHieivyfiMJqgtPh8rqegPsIgIPzEGW4130_provenance.