@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U
> .
@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/v3.0.0/void/
> .
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_head
{
this:
np:hasAssertion
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_assertion
;
np:hasProvenance
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_provenance
;
np:hasPublicationInfo
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_assertion
a
np:Assertion
.
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_provenance
a
np:Provenance
.
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C1861172
a
ncit:C7057
.
dgn-gda:DGN8833a0bc19921b85e910eb0a4b2f38f6
sio:SIO_000628
miriam-gene:2147
,
lld:C1861172
;
a
sio:SIO_001122
.
}
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_provenance
{
dgn-np:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_assertion
dcterms:description
"[Carriership of FV Leiden or FII A20210 mutations identifies an at-risk condition for venous thrombosis in the lower extremities, SVT or CVT. In patients with SVT, screening for the JAK2 V617F mutation may be useful in recognising patients who should be ca]. 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:17307838
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP53118.RAdoCgQ3RbcTqPDGtu00YCYI6Cb3y_wL9dZH4Knzqp_7U130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:09+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}