@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A
> .
@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:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_head
{
this:
np:hasAssertion
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_assertion
;
np:hasProvenance
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_provenance
;
np:hasPublicationInfo
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_assertion
a
np:Assertion
.
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_provenance
a
np:Provenance
.
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_assertion
{
miriam-gene:27185
a
ncit:C16612
.
lld:C0036337
a
ncit:C7057
.
dgn-gda:DGN195f2712556034e883105877e0924652
sio:SIO_000628
miriam-gene:27185
,
lld:C0036337
;
a
sio:SIO_001121
.
}
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_provenance
{
dgn-np:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_assertion
dcterms:description
"[Disrupted in schizophrenia 1 (DISC1) has been associated with risk of schizophrenia, schizoaffective disorder, bipolar disorder, major depression, autism and Asperger syndrome, but apart from in the original translocation family, true causal variants have yet to be confirmed.]. 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:18317464
;
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:NP752216.RAy1Jb6IDRQ2DzBV_ypIrehs4PCPRwVHVRx_BxtICMD9A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}