@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w
> .
@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:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_head
{
this:
np:hasAssertion
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_assertion
;
np:hasProvenance
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_provenance
;
np:hasPublicationInfo
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_assertion
a
np:Assertion
.
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_provenance
a
np:Provenance
.
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_assertion
{
miriam-gene:729230
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN6108ac338e2d12718c686359e10a5110
sio:SIO_000628
miriam-gene:729230
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_provenance
{
dgn-np:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_assertion
dcterms:description
"[V64Ile polymorphism in CCR2 has been implicated in the manifestation of myocardial infarction in different populations, but data on association of the CCR5 deletion variant in etiology of CAD are conflicting.]. 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:17383752
;
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:NP932366.RAj5oHf5hkb-ssI5s3ojnAydzY7rDASr3TZeLnOIPJO8w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}