@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g
> .
@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:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_head
{
this:
np:hasAssertion
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_assertion
;
np:hasProvenance
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_provenance
;
np:hasPublicationInfo
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_assertion
a
np:Assertion
.
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_provenance
a
np:Provenance
.
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0398623
a
ncit:C7057
.
dgn-gda:DGN1a5888880bc50d7962ed7a9a21d11964
sio:SIO_000628
miriam-gene:3717
,
lld:C0398623
;
a
sio:SIO_001121
.
}
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_provenance
{
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_assertion
dcterms:description
"[Accordingly, it seems that the investigation for the V617F mutation of the JAK2 gene is not mandatory in all Mexican mestizo patients with unexplained thrombophilia and that this genetic study should be reserved for special cases, such as patients with thrombosis in uncommon sites or patients with cell counts suggesting the presence of an underlying MPD.]. 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:18796251
;
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:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}