@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q
> .
@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:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_head
{
this:
np:hasAssertion
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_assertion
;
np:hasProvenance
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_assertion
a
np:Assertion
.
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_provenance
a
np:Provenance
.
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_assertion
{
miriam-gene:23245
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGNab7ddbb757f2d18c1f28acb8e4b0935a
sio:SIO_000628
miriam-gene:23245
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_provenance
{
dgn-np:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_assertion
dcterms:description
"[Among these de novo and rare inherited CNVs, there were also examples of genes (ASTN2, GABRG1, and CNTN5) previously implicated by rare CNVs in other neurodevelopmental conditions including autism spectrum disorder (ASD).]. 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:21832240
;
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:NP491394.RAuFc0tcxzPDxBpUOupaaa8OYz8nDVM0uv7nvzbKSqv5Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}