Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.
- NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_assertion description "[Most ASDs have a genetic origin and one gene recently implicated in the etiology of autism is the Deleted-In-Autism-1 (DIA1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.
- NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_assertion evidence source_evidence_literature NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.
- NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_assertion SIO_000772 21264219 NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.
- NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_assertion wasDerivedFrom befree-2016 NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.
- NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_assertion wasGeneratedBy ECO_0000203 NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.
- befree-2016 importedOn "2016-02-19" NP867498.RAJAVMxDNfP8ajXAxXkqi0q0gs1sqky3J5054wVrFn6Ic130_provenance.