@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso
> .
@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:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_head
{
this:
np:hasAssertion
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_assertion
;
np:hasProvenance
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_provenance
;
np:hasPublicationInfo
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_assertion
a
np:Assertion
.
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_provenance
a
np:Provenance
.
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_assertion
{
miriam-gene:3953
a
ncit:C16612
.
lld:C0162739
a
ncit:C7057
.
dgn-gda:DGN33a0f902b1c4ba81c8a5d3377e75672e
sio:SIO_000628
miriam-gene:3953
,
lld:C0162739
;
a
sio:SIO_001122
.
}
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_provenance
{
dgn-np:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_assertion
dcterms:description
"[Although certain LEPR haplotypes are more frequent in HELLP syndrome, we conclude that there is no compelling evidence that the four studied LEPR SNP polymorphisms associated with the development of HELLP syndrome.]. 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:20149225
;
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:NP85099.RAnJ6gK1pb5IvUb9rIvQfoo8CuxrsxLxnmyvInanbUeso130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}