@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4
> .
@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:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_head
{
this:
np:hasAssertion
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_assertion
;
np:hasProvenance
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_provenance
;
np:hasPublicationInfo
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_assertion
a
np:Assertion
.
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_provenance
a
np:Provenance
.
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_assertion
{
miriam-gene:23564
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN0dfb508469b6590923893ca620c67f6d
sio:SIO_000628
miriam-gene:23564
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_provenance
{
dgn-np:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_assertion
dcterms:description
"[The discovery of a functional polymorphism within the DDAH2 promoter suggests that there may be common, individual differences in the ability to metabolise ADMA in vivo, that in turn, might underlie susceptibility to cardiovascular disease.]. 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:14550280
;
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:NP747670.RAUlOlvsatmNO4gc2EScKja8O_pjWbLd-4g4xmajFsR_4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}