Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.
- NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_assertion description "[A large number of these corresponded to genomic regions or genes (ATP13A4, CDH9, CDH13, CNTNAP2, CTNNA3, DIAPH3, GRIN2A, MDGA2, SHANK3) that have been either associated with ASD for most of them, or involved in speech or language impairment, or in RE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.
- NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_assertion evidence source_evidence_literature NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.
- NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_assertion SIO_000772 22738016 NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.
- NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_assertion wasDerivedFrom befree-20150227 NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.
- NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_assertion wasGeneratedBy ECO_0000203 NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977230.RAeqBsotHBlli9v-QCSkZM6uWIKcBwuS5c24pJ8iC1rcE130_provenance.