@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_head
{
this:
np:hasAssertion
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_assertion
;
np:hasProvenance
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_provenance
;
np:hasPublicationInfo
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_assertion
a
np:Assertion
.
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_provenance
a
np:Provenance
.
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C0155773
a
ncit:C7057
.
dgn-gda:DGN6137f263f8a13b663646ea3c84dde0cc
sio:SIO_000628
miriam-gene:7450
,
lld:C0155773
;
a
sio:SIO_001121
.
}
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_provenance
{
dgn-np:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_assertion
dcterms:description
"[We describe a significant proportion of individual TS females having high levels of vWF, factor VIII, fibrinogen and CRP (15-40%) and an increased frequency of the Leiden mutation, with important associations with CIMT and blood pressure, suggesting that a subset of TS may have an unfavourable haemostatic balance, which may contribute to the increased risk of premature ischaemic heart disease and possibly increase the risk of deep venous and portal vein thrombosis.]. 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:21848660
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP917610.RAe8zMUHxM9-77Vq99-SkgNRbiv-eeyLKeu4f-GxT9u1U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:40+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}