@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w
> .
@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:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_head
{
this:
np:hasAssertion
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_assertion
;
np:hasProvenance
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_provenance
;
np:hasPublicationInfo
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_assertion
a
np:Assertion
.
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_provenance
a
np:Provenance
.
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_assertion
{
miriam-gene:414
a
ncit:C16612
.
lld:C0567439
a
ncit:C7057
.
dgn-gda:DGN0886e27f5949a8e4e673647314b66aa3
sio:SIO_000628
miriam-gene:414
,
lld:C0567439
;
a
sio:SIO_001121
.
}
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_provenance
{
dgn-np:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_assertion
dcterms:description
"[Some of the genes located in ASD-specific copy number variants act in common pathways, most notably the phosphatidylinositol signaling and the glutamatergic synapse, both known to be affected in several genetic syndromes related with autism and previously associated with 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:19246517
;
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:NP765935.RA4tZfn9lea9lGknLwkwimZ4BbexNM1a3Ffqjr9IZ7v1w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}