@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E
> .
@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:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_head
{
this:
np:hasAssertion
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_assertion
;
np:hasProvenance
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_assertion
a
np:Assertion
.
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_provenance
a
np:Provenance
.
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_assertion
{
miriam-gene:5327
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN7ea52238f9fd05480711ea207506e683
sio:SIO_000628
miriam-gene:5327
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_provenance
{
dgn-np:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_assertion
dcterms:description
"[The observed allele frequencies of the polymorphisms of t-PA, fibrinogen, FVII, ACE, angiotensinogen and the plasma levels of PAI-1 and D-Dimer were in accordance with the low CVD risk in the Inuit, considering the observed associations between these measures and CVD risk in Caucasian populations, but for other measures this was not the case (allele frequencies of the PAI-1 polymorphism, and plasma levels of fibrinogen, FVII and t-PA).]. 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:10235437
;
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:NP248857.RAUrRokQM7cKzxa2LkMpwdnb3IqoqLg9BMQ-XBlxO2y3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}