Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.
- NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_assertion description "[Here we have addressed the allelic diversity of the DISC1, DISC2 and TRAX genes, clustered in 1q42, in Finnish families ascertained for infantile autism (97 families, n(affected)=138) and Asperger syndrome (29 families, n(affected)=143).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.
- NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_assertion evidence source_evidence_literature NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.
- NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_assertion SIO_000772 17579608 NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.
- NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_assertion wasDerivedFrom befree-2016 NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.
- NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_assertion wasGeneratedBy ECO_0000203 NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.
- befree-2016 importedOn "2016-02-19" NP616025.RASfdEqS19l7cuz8YxUj8W0kMCcuQbx7n1Uk3XvYrGe6s130_provenance.