@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ
> .
@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:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_head
{
this:
np:hasAssertion
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_assertion
;
np:hasProvenance
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_assertion
a
np:Assertion
.
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_provenance
a
np:Provenance
.
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0398623
a
ncit:C7057
.
dgn-gda:DGNe30a6ad5daa23bad3e2f2439339dfede
sio:SIO_000628
miriam-gene:5660
,
lld:C0398623
;
a
sio:SIO_001121
.
}
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_provenance
{
dgn-np:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_assertion
dcterms:description
"[Considering the increased risks with the association between VTE and the higher prevalence of PC and PS deficiencies, TT genotype mutations and high level of fibrinogen, it is advisable to perform a complete thrombophilia screening in TS patients before starting HRT.]. 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:21586893
;
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:NP232446.RAeV-K2L1X5SSxOgGRsigtVOnmD02iTxgd0xD7SoGITXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}