@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM
> .
@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:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_head
{
this:
np:hasAssertion
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_assertion
;
np:hasProvenance
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_provenance
;
np:hasPublicationInfo
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_assertion
a
np:Assertion
.
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_provenance
a
np:Provenance
.
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNf0d426961579fd6d40d23c9d121bc623
sio:SIO_000628
miriam-gene:5660
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_provenance
{
dgn-np:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_assertion
dcterms:description
"[Common genetic polymorphisms in European-Ancestry populations, such as factor V Leiden and prothrombin G20210A, and environmental risk factors, such as obesity, may account for some of the increased risk in European populations, and high factor VIII, high von Willebrand factor and low protein C levels and increased prevalence of obesity may explain some of the increased risk in African-Americans.]. 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:21797965
;
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:NP677647.RA3tcDXgkvtLC3SSwiVr3DP3ig69x70DqwVaKtWGOE6vM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}