@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k
> .
@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:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_head
{
this:
np:hasAssertion
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_assertion
;
np:hasProvenance
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_provenance
;
np:hasPublicationInfo
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_assertion
a
np:Assertion
.
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_provenance
a
np:Provenance
.
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_assertion
{
miriam-gene:11214
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN4223138a5c0a1698bbd44ad85fc31318
sio:SIO_000628
miriam-gene:11214
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_provenance
{
dgn-np:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_assertion
dcterms:description
"[The GWAS for aPTT was conducted in 9,240 individuals of European ancestry from the Atherosclerosis Risk in Communities (ARIC) study, and the GWAS for PT was conducted in 2,583 participants from the Genetic Study of Three Population Microisolates in South Tyrol (MICROS) and the Lothian Birth Cohorts (LBC) of 1921 and 1936.]. 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:22703881
;
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:NP443867.RAiiKhSU0XR30vCAXO9H7NqhqVV5QViKEohD-QUVaaK4k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}