@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg
> .
@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:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_head
{
this:
np:hasAssertion
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_assertion
;
np:hasProvenance
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_provenance
;
np:hasPublicationInfo
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_assertion
a
np:Assertion
.
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_provenance
a
np:Provenance
.
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_assertion
{
miriam-gene:653361
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN99de7198f532b5c84f8efdab698e0a23
sio:SIO_000628
miriam-gene:653361
,
lld:C0038454
;
a
sio:SIO_001122
.
}
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_provenance
{
dgn-np:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_assertion
dcterms:description
"[To investigate the relationship between C923T (Ala308Val) polymorphism in exon 10 of protein 47000 phagocyte oxidase(p47(phox)) gene and stroke and to evaluate the effect of C923T (Ala308Val) polymorphism on plasma lipid levels in Hunan Hans population.]. 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:17922419
;
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:NP69139.RAy-D4_d-TrVj8QnTBgTjNZtQn-ref1JNacPlkI8Qkndg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:33+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" .
}