@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY
> .
@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:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_head
{
this:
np:hasAssertion
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_assertion
;
np:hasProvenance
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_provenance
;
np:hasPublicationInfo
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_assertion
a
np:Assertion
.
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_provenance
a
np:Provenance
.
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0040053
a
ncit:C7057
.
dgn-gda:DGN747fcda15c03b925e7f296ac9d9fd8b2
sio:SIO_000628
miriam-gene:5624
,
lld:C0040053
;
a
sio:SIO_001122
.
}
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_provenance
{
dgn-np:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_assertion
dcterms:description
"[individuals carrying the 4600AG EPCR genotype have high sEPCR levels but do not have an increased risk of thrombosis, whereas individuals carrying the 4678CC genotype have higher APC levels and lower risk of venous thromboembolism ]. 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:15116250
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP134451.RAxeZWP-dzJp9QpyMQOwIHrYbYfNl_g1DRU7BmUIhV1kY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:10+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" .
}