@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE
> .
@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:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_head
{
this:
np:hasAssertion
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_assertion
;
np:hasProvenance
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_provenance
;
np:hasPublicationInfo
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_assertion
a
np:Assertion
.
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_provenance
a
np:Provenance
.
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_assertion
{
miriam-gene:84152
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNd78d68e1174bc9bad066ca7b376885bc
sio:SIO_000628
miriam-gene:84152
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_provenance
{
dgn-np:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_assertion
dcterms:description
"[Recent work on DAOA, PPP1R1B, and APOL1 suggests that these genes present common alleles associated to increase risk of schizophrenia but conferring an overall selective advantage, related to better cognitive performance (DAOA and PPP1R1B) or protection against pathogens (APOL1).]. 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:20483474
;
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:NP66301.RAiC2JCVjfvhZTizGZHTRfssFyLq_KAI-YoxKZUVlDlnE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}