@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4
> .
@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:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_head
{
this:
np:hasAssertion
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_assertion
;
np:hasProvenance
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_provenance
;
np:hasPublicationInfo
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_assertion
a
np:Assertion
.
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_provenance
a
np:Provenance
.
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_assertion
{
miriam-gene:10544
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN9fe12c2df5ae50a24b4cfbdd561f46e9
sio:SIO_000628
miriam-gene:10544
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_provenance
{
dgn-np:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_assertion
dcterms:description
"[These data indicate that individuals carrying the 4600AG 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: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:NP624114.RAaGOOqWAG_mhw5kP0vnBqvfQcNexJWXjFVYtO-JTWql4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}