@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk
> .
@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:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_head
{
this:
np:hasAssertion
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_assertion
;
np:hasProvenance
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_provenance
;
np:hasPublicationInfo
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_assertion
a
np:Assertion
.
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_provenance
a
np:Provenance
.
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_assertion
{
miriam-gene:10544
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGNe4b3c8230ef32f9511db841984a95387
sio:SIO_000628
miriam-gene:10544
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_provenance
{
dgn-np:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_assertion
dcterms:description
"[These results show that in 20210A carriers the venous thromboembolism risk is influenced both by the actual prothrombin levels and by the EPCR A3 haplotype, via its effect on sEPCR 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:18403391
;
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:NP728841.RARPBAvfLfYEqGLK5fqdMVwaWr58Pz0AP5CSPJyeViRYk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+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" .
}