@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0
> .
@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:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_head
{
this:
np:hasAssertion
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_assertion
;
np:hasProvenance
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_provenance
;
np:hasPublicationInfo
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_assertion
a
np:Assertion
.
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_provenance
a
np:Provenance
.
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_assertion
{
miriam-gene:125
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN531d43097a7bb3203163172c2278a1a4
sio:SIO_000628
miriam-gene:125
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_provenance
{
dgn-np:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_assertion
dcterms:description
"[The mutant genotypes of eNOS gene T-786C mutation and the fast form of ADH2 Arg47His polymorphism had an additive interaction on the risk of premature CAD in Chinese population. Further investigations with big sample size are necessary for confirming this additive interaction.]. 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:17289126
;
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:NP63527.RAUeBv1KdiY8_jYnvUH74mC-kz7nYEIK9DJ0-TLP82UF0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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: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" .
}