@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A130_assertion
a
np:Assertion
.
dgn-np:NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A130_provenance
a
np:Provenance
.
dgn-np:NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:404677
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGNfb56519ae254291a5c7c5315eda75cf1
sio:SIO_000628
miriam-gene:404677
,
lld:C0010054
;
a
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.
}
dgn-np:NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A130_provenance
{
dgn-np:NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A130_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
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sio:SIO_000772
miriam-pubmed:21848660
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP378386.RAxnEQBO-YSDQupPZ2jhR-Rfrsju_UsAyTAeGEKJgS11A130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
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pav:createdBy
<
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