@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0
> .
@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:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_head
{
this:
np:hasAssertion
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_assertion
;
np:hasProvenance
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_provenance
;
np:hasPublicationInfo
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_assertion
a
np:Assertion
.
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_provenance
a
np:Provenance
.
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_assertion
{
miriam-gene:2903
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGNe52da5ea65ce3c03f72522616a79df1b
sio:SIO_000628
miriam-gene:2903
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_provenance
{
dgn-np:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_assertion
dcterms:description
"[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. 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:22833210
;
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:NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}