Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.
- NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_assertion description "[The results of this study showed that the vast majority of all individuals with 22q11 deletion syndrome have behavior and/or learning problems and more than 40% meet criteria for either ASD, ADHD or both.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.
- NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_assertion evidence source_evidence_literature NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.
- NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_assertion SIO_000772 19070990 NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.
- NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_assertion wasDerivedFrom befree-2016 NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.
- NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_assertion wasGeneratedBy ECO_0000203 NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.
- befree-2016 importedOn "2016-02-19" NP708293.RAoexYAo68oNyRUSh408fRcCmZ4i2aihkjACK1sm7aUIU130_provenance.