@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic
> .
@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:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_head
{
this:
np:hasAssertion
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_assertion
;
np:hasProvenance
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_provenance
;
np:hasPublicationInfo
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_assertion
a
np:Assertion
.
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_provenance
a
np:Provenance
.
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0013537
a
ncit:C7057
.
dgn-gda:DGN4cde29902b6f3c0905369700721a6866
sio:SIO_000628
miriam-gene:4846
,
lld:C0013537
;
a
sio:SIO_001121
.
}
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_provenance
{
dgn-np:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_assertion
dcterms:description
"[We analyzed the Glu298Asp polymorphism of the endothelial nitric oxide synthase gene and asymmetric dimethylarginine (ADMA) in 55 Turkish patients with PE without fetal growth retardation (FGR) and in 54 healthy pregnant women.]. 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:20598027
;
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:NP585700.RARL_EIjHCkNQqPGs8mFPVOC0pPThWpcSPhCEoAT1vDic130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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" .
}