@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y
> .
@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:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_head
{
this:
np:hasAssertion
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_assertion
;
np:hasProvenance
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_assertion
a
np:Assertion
.
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_provenance
a
np:Provenance
.
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_assertion
{
miriam-gene:116443
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN2aafbfb6e77ae8457d9f587129cdf7d2
sio:SIO_000628
miriam-gene:116443
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_provenance
{
dgn-np:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_assertion
dcterms:description
"[Although the functional significance of these mutations remains to be characterized, our study indicates that rare mutations in the GRIN3A gene may contribute to the pathogenesis of schizophrenia in certain patients.]. 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:19665356
;
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:NP692561.RAmu6huSlIR5b_RTenLvmWQFVkSbhDDW8tqoHsyviRl4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}