@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_head
{
this:
np:hasAssertion
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_assertion
;
np:hasProvenance
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_provenance
;
np:hasPublicationInfo
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_assertion
a
np:Assertion
.
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_provenance
a
np:Provenance
.
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_assertion
{
miriam-gene:93986
a
ncit:C16612
.
lld:C0023009
a
ncit:C7057
.
dgn-gda:DGN9ed367054759ff79f9307fee72109ee0
sio:SIO_000628
miriam-gene:93986
,
lld:C0023009
;
a
sio:SIO_001121
.
}
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_provenance
{
dgn-np:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_assertion
dcterms:description
"[CNTNAP2 is known to be involved in the cause of language and speech disorders and autism spectrum disorder and is in the same pathway as FOXP2, another important language gene, which makes it a candidate gene for causal studies speech and language disorders such as stuttering.]. 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:21108403
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP432099.RAiJylrSSxkWoATyGgyOTwm7w3r2ztgiU7Fg9FHUCwwU4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}