@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk
> .
@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:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_head
{
this:
np:hasAssertion
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_assertion
;
np:hasProvenance
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_provenance
;
np:hasPublicationInfo
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_assertion
a
np:Assertion
.
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_provenance
a
np:Provenance
.
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_assertion
{
miriam-gene:4929
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN613db1cb18025b5577b2b2eb7534a7c3
sio:SIO_000628
miriam-gene:4929
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_provenance
{
dgn-np:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_assertion
dcterms:description
"[The study failed to identify any of the described mutations in patients or controls. Nevertheless, these negative results do not exclude altered expression of nuclear receptors in schizophrenia or the presence of other mutations.]. 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:15211629
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP53607.RAX1_HEXMR9sIkWSto4QXqjOYciBMKGM6-jXp_PRW5mMk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}