Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.
- NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion description "[Synaptic genes, NLGN3 and NLGN4X, two homologous members of the neuroligin family, have been supposed as predisposition loci for autism spectrum disorders (ASDs), and defects of these two genes have been identified in a small fraction of individuals with ASDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.
- NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion evidence source_evidence_literature NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.
- NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion SIO_000772 21569590 NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.
- NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion wasDerivedFrom befree-20140225 NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.
- NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion wasGeneratedBy ECO_0000203 NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance.