@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA
> .
@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/v4.0.0/void/
> .
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_head
{
this:
np:hasAssertion
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_assertion
;
np:hasProvenance
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_provenance
;
np:hasPublicationInfo
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_assertion
a
np:Assertion
.
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_provenance
a
np:Provenance
.
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN433601a709eac74164081fdc33427746
sio:SIO_000628
miriam-gene:2147
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_provenance
{
dgn-np:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP665142.RA7P3Plyh4g5Eai0coUT1f9mXXkYg1AQ6cUgYUcdBs0MA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:47+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}