@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_head
{
this:
np:hasAssertion
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_assertion
;
np:hasProvenance
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_provenance
;
np:hasPublicationInfo
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_assertion
a
np:Assertion
.
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_provenance
a
np:Provenance
.
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_assertion
{
miriam-gene:414
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNf519b5e5d76f72864631813f03e4bb34
sio:SIO_000628
miriam-gene:414
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_provenance
{
dgn-np:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP722818.RAV0OFuPpHLObUl5hyxIcffQWIufw5NLWf0cfufm74ido130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:12+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}