Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_assertion description "[A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_assertion evidence source_evidence_literature NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_assertion SIO_000772 21569590 NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_assertion wasDerivedFrom befree-2016 NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_assertion wasGeneratedBy ECO_0000203 NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.
- befree-2016 importedOn "2016-02-19" NP893955.RAPOqzE0QXct8N2ChMxmCq5Qp4XVAlwIt25ynk0Lhll5s130_provenance.