Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_assertion description "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_assertion evidence source_evidence_literature NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_assertion SIO_000772 19565319 NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_assertion wasDerivedFrom befree-20140225 NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_assertion wasGeneratedBy ECO_0000203 NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.