@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk
> .
@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:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_head
{
this:
np:hasAssertion
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_assertion
;
np:hasProvenance
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_provenance
;
np:hasPublicationInfo
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_assertion
a
np:Assertion
.
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_provenance
a
np:Provenance
.
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_assertion
{
miriam-gene:5554
a
ncit:C16612
.
lld:C0004943
a
ncit:C7057
.
dgn-gda:DGN1dcc206afffeb868c66e0f68182fcad2
sio:SIO_000628
miriam-gene:5554
,
lld:C0004943
;
a
sio:SIO_001121
.
}
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_provenance
{
dgn-np:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_assertion
dcterms:description
"[These findings indicate that the H1 haplotype protects Behçet's patients from thrombosis, likely via increased levels of activated protein C, whereas individuals carrying the H3 haplotype seem to be protected from the clinical manifestations associated with Behçet's disease, probably via increased soluble endothelial protein C levels.]. 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:21851971
;
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:NP353861.RA5CPyhJayo_8lbmidH2FzTSK0CPhCdqnbDoY7GRlDuWk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}