@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk
> .
@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 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:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_head
{
this:
np:hasAssertion
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_assertion
;
np:hasProvenance
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_provenance
;
np:hasPublicationInfo
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_assertion
a
np:Assertion
.
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_provenance
a
np:Provenance
.
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0149871
a
ncit:C7057
.
dgn-gda:DGNf1ecf6dda8e6748ef71f874652687e86
sio:SIO_000628
miriam-gene:2147
,
lld:C0149871
;
a
sio:SIO_001122
.
}
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_provenance
{
dgn-np:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_assertion
dct:description
"[As gene variants predisposing to thrombophilia and influencing the increased risk of vein thrombosis might influence response to local thrombolysis, the aim of the work was to characterize the pharmacogenetic conditions for local streptokinase treatment in patients with a deep vein thrombosis (DVT) of lower extremities based on the following polymorphism analyses: G1691A polymorphism of factor V (FV), G20210A polymorphism of prothrombin (PT), A4250G (Thr312Ala) polymorphism of fibrinogen-alpha (FGA), G(-455)A polymorphism of fibrinogen-beta (FGB), 4G/5G polymorphism of plasminogen activator inhibitor type 1(PAI-1) and insertion/deletion (I/D) polymorphism of tissue plasminogen activator (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:16466010
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44561.RAsKxbomuGxBq1yzy6Tcy_gqP6frU0kaykweem9Vf-nxk130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}