@prefix orcid: .
@prefix this: .
@prefix rdfs: .
@prefix xsd: .
@prefix sio: .
@prefix ncit: .
@prefix lld: .
@prefix miriam-gene: .
@prefix miriam-pubmed: .
@prefix eco: .
@prefix wi: .
@prefix prov: .
@prefix pav: .
@prefix prv: .
@prefix dcterms: .
@prefix np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_head {
this: np:hasAssertion dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_assertion;
np:hasProvenance dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_provenance;
np:hasPublicationInfo dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_publicationInfo;
a np:Nanopublication .
dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_assertion a np:Assertion .
dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_provenance a np:Provenance .
dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_publicationInfo a
np:PublicationInfo .
}
dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_assertion {
miriam-gene:414 a ncit:C16612 .
lld:C0004352 a ncit:C7057 .
dgn-gda:DGN778ab30fea874e34dd5987bd20c35d72 sio:SIO_000628 miriam-gene:414, lld:C0004352;
a sio:SIO_001121 .
}
dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_provenance {
dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_assertion dcterms:description
"[Nearly half of the 683 identified DEGs are expressed in the brain (P = 0.003), and a significant number of them are involved in mechanisms previously associated with ASD such as protein synthesis, cytoskeleton regulation, cellular adhesion and alternative splicing, which validate the use of SHEDs to disentangle the causes of autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
wi:evidence dgn-void:source_evidence_literature;
sio:SIO_000772 miriam-pubmed:23801657;
prov:wasDerivedFrom dgn-void:befree-20150227;
prov:wasGeneratedBy eco:ECO_0000203 .
dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date .
dgn-void:source_evidence_literature a eco:ECO_0000212;
rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP253324.RAvKR_S-YBO83vlKYzNV90wS2ECVQb-3qQh-LFJQ5H8aQ130_publicationInfo {
this: dcterms:created "2015-08-25T14:40:04+02:00"^^xsd:dateTime;
dcterms:rights ;
dcterms:rightsHolder dgn-void:IBIGroup;
dcterms:subject sio:SIO_000983;
prv:usedData dgn-void:disgenetv3.0rdf;
pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
pav:createdBy orcid:0000-0003-0169-8159;
pav:version "v3.0.0.0" .
dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}