Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.
- NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_assertion description "[A large number of these corresponded to genomic regions or genes (ATP13A4, CDH9, CDH13, CNTNAP2, CTNNA3, DIAPH3, GRIN2A, MDGA2, SHANK3) that have been either associated with ASD for most of them, or involved in speech or language impairment, or in RE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.
- NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_assertion evidence source_evidence_literature NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.
- NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_assertion SIO_000772 22738016 NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.
- NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_assertion wasDerivedFrom befree-2016 NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.
- NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_assertion wasGeneratedBy ECO_0000203 NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.
- befree-2016 importedOn "2016-02-19" NP993459.RAZ3z4TsBvyqIJlT5IwQpIdtMPZVOUZPLVR5OmbU4fx-k130_provenance.