@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q
> .
@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:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_head
{
this:
np:hasAssertion
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_assertion
;
np:hasProvenance
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_assertion
a
np:Assertion
.
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_provenance
a
np:Provenance
.
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGNc9c20228f6c3b3d4f41c95a1c71d6997
sio:SIO_000628
miriam-gene:3717
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_provenance
{
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_assertion
dcterms:description
"[Furthermore, patients affected by essential thrombocythemia who are carriers of the Janus kinase 2 Val617Phe mutation show a higher incidence of venous thromboembolism both before, and at the time of diagnosis, compared with noncarriers, and recent evidence of splanchnic and cerebral vein thrombosis in carriers of the Janus kinase 2 Val617Phe mutation has been reported.]. 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:18600099
;
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:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}