Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.
- NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_assertion description "[Notwithstanding complexities, our results further implicate the SHANK3-NLGN4-NRXN1 postsynaptic density genes and also identify novel loci at DPP6-DPP10-PCDH9 (synapse complex), ANKRD11, DPYD, PTCHD1, 15q24, among others, for a role in ASD susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.
- NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_assertion evidence source_evidence_literature NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.
- NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_assertion SIO_000772 18252227 NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.
- NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_assertion wasDerivedFrom befree-2016 NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.
- NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_assertion wasGeneratedBy ECO_0000203 NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.
- befree-2016 importedOn "2016-02-19" NP653967.RACgVmSnBAXciIXR0eDYdMKadSI7pdG0ND6vt9NJETyKo130_provenance.