@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_head
{
this:
np:hasAssertion
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_assertion
;
np:hasProvenance
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_provenance
;
np:hasPublicationInfo
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_assertion
a
np:Assertion
.
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_provenance
a
np:Provenance
.
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_assertion
{
miriam-gene:79001
a
ncit:C16612
.
lld:C0151744
a
ncit:C7057
.
dgn-gda:DGN17efe496219013dd51e129682a97e7d5
sio:SIO_000628
miriam-gene:79001
,
lld:C0151744
;
a
sio:SIO_001122
.
}
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_provenance
{
dgn-np:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_assertion
dcterms:description
"[the discrepant association findings in Chinese and German populations may be explained by ethnic differences in genetic and perhaps environmental predisposition, modifying the polygenic CHD phenotype by interacting with VKORC1 variants and thus conferring]. 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:17549303
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP86372.RAG2Qi2Kzr4JGHpA0kzIOCpln-ZVMX5yCBCqx0SOqSPko130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:27+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}