Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.
- NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_assertion description "[Interestingly, the patient with decreased KIAA2022 expression had only mild ID with severe language delay and repetitive behaviors falling in the range of an autism spectrum disorder (ASD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.
- NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_assertion evidence source_evidence_literature NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.
- NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_assertion SIO_000772 23615299 NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.
- NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_assertion wasDerivedFrom befree-20140225 NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.
- NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_assertion wasGeneratedBy ECO_0000203 NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP698906.RA3aY7enTgLoDPllnGn8AXyrg1yfBLGdaMcDyZxBtrg9A130_provenance.