@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_head
{
this:
np:hasAssertion
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_assertion
;
np:hasProvenance
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_provenance
;
np:hasPublicationInfo
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_assertion
a
np:Assertion
.
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_provenance
a
np:Provenance
.
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_assertion
{
miriam-gene:4973
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNfe1d0870b4b12c64e3320a2f68163081
sio:SIO_000628
miriam-gene:4973
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_provenance
{
dgn-np:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_assertion
dcterms:description
"[The OLR1 expression was significantly lower in AD cases bearing the CC and CT genotypes compared with controls with the same genotypes. In conclusion, our data suggest that genetic variation in the OLR1 gene may modify the risk of AD.]. 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:12807963
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP67011.RAbxjBboLAS3VA3d9RAzd8SBBaE_qpbc9FiHNOaSfkK2c130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:16+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}