Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.
- NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_assertion description "[High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.
- NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_assertion evidence source_evidence_literature NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.
- NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_assertion SIO_000772 19401682 NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.
- NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_assertion wasDerivedFrom gad-20130706 NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.
- NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_assertion wasGeneratedBy ECO_0000203 NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.
- gad-20130706 importedOn "2013-07-06" NP78766.RAcNY9VKWKxkdTjaPDDED-w5RWa8WJqGhPvMT-ioDCmfs130_provenance.