@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc
> .
@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:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_head
{
this:
np:hasAssertion
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_assertion
;
np:hasProvenance
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_provenance
;
np:hasPublicationInfo
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_assertion
a
np:Assertion
.
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_provenance
a
np:Provenance
.
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_assertion
{
miriam-gene:4695
a
ncit:C16612
.
lld:C0155626
a
ncit:C7057
.
dgn-gda:DGN12defa2731cdab7f6c857564b34acdbd
sio:SIO_000628
miriam-gene:4695
,
lld:C0155626
;
a
sio:SIO_001121
.
}
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_provenance
{
dgn-np:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_assertion
dcterms:description
"[The frequencies of T allele and T/T homozygotes in patients with AMI were significantly higher than in controls and in patients with angina without prior AMI, suggesting that the CD14 promoter polymorphism is associated with AMI rather than with coronary atherosclerosis, and this polymorphism may be one of the genetic risk factors for AMI in Japanese men.]. 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:10980225
;
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:NP647035.RAg7ngXZ9kdLOnELPhZWNLQOXRPU3oXkPf_XxbgfTScyc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}