@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4
> .
@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/v3.0.0/void/
> .
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_head
{
this:
np:hasAssertion
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_assertion
;
np:hasProvenance
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_provenance
;
np:hasPublicationInfo
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_assertion
a
np:Assertion
.
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_provenance
a
np:Provenance
.
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0034065
a
ncit:C7057
.
dgn-gda:DGNa8034d34b302b1d4d4d26210bfd8ed47
sio:SIO_000628
miriam-gene:4524
,
lld:C0034065
;
a
sio:SIO_001122
.
}
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_provenance
{
dgn-np:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_assertion
dcterms:description
"[The FVL is statistically more frequent in patients with PE compared to the control group, and the frequency of FVL, FII, and MTHFR is not significantly higher in patients with acute PE who have no obvious risk factors compared to those with obvious risk factors.]. 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:19618008
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP91452.RAagh0IGvbrv0f9VGbBVrZp3s3QNAY8t6IWePL8nqsee4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:30+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}