@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c
> .
@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:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_head
{
this:
np:hasAssertion
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_assertion
;
np:hasProvenance
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_assertion
a
np:Assertion
.
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_provenance
a
np:Provenance
.
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C0032914
a
ncit:C7057
.
dgn-gda:DGN97a87be563c3af30612c806026bdf893
sio:SIO_000628
miriam-gene:2147
,
lld:C0032914
;
a
sio:SIO_001122
.
}
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_provenance
{
dgn-np:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_assertion
dcterms:description
"[ We didn't find any difference in the prevalence of genetic mutations in patients with preeclampsia compared to the control group. The prevalence of APC resistance was statistically higher in preeclamptic patients compared to the control group.]. 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:12879654
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44499.RATdVS_G2VhFwEXrZsrvXBYT9Kmn9DLeXJAilM6bEoD3c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}