@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8
> .
@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:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_head
{
this:
np:hasAssertion
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_assertion
;
np:hasProvenance
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_provenance
;
np:hasPublicationInfo
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_assertion
a
np:Assertion
.
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_provenance
a
np:Provenance
.
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN8ac45aabb4455e411c4692384e88eb8a
sio:SIO_000628
miriam-gene:8170
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_provenance
{
dgn-np:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_assertion
dcterms:description
"[Here, we describe an association of the 3'-UTR +1073 C/T polymorphism of the OLR1 (oxidised LDL receptor 1) on chromosome 12 with AD in French sporadic (589 cases and 663 controls) and American familial (230 affected sibs and 143 unaffected sibs) populations.]. 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: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:NP296903.RA-rUkO6Fm2zSX8UdLH-DcCwoP-h62-I03RPthvWHaOA8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}