Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.
- NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_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." NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.
- NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_assertion evidence source_evidence_literature NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.
- NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_assertion SIO_000772 23918416 NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.
- NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_assertion wasDerivedFrom befree-20150227 NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.
- NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_assertion wasGeneratedBy ECO_0000203 NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434661.RAWoVCqrOiSOJ8418HnhqD8NCA3yO_76V_i_evqJVN_9Q130_provenance.