Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.
- NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_assertion description "[GRIN2B alterations, including mutation and gene disruption by apparently balanced chromosomal rearrangements, have been described in patients with intellectual disability and autism spectrum disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.
- NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_assertion evidence source_evidence_literature NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.
- NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_assertion SIO_000772 23918416 NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.
- NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_assertion wasDerivedFrom befree-2016 NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.
- NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_assertion wasGeneratedBy ECO_0000203 NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.
- befree-2016 importedOn "2016-02-19" NP1099798.RAHpRN_vZWhafH_mqh7OWXLA5radwocqmIcrqIRLBUOek130_provenance.