@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU
> .
@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/v4.0.0/void/
> .
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_head
{
this:
np:hasAssertion
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_assertion
;
np:hasProvenance
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_provenance
;
np:hasPublicationInfo
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_assertion
a
np:Assertion
.
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_provenance
a
np:Provenance
.
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN7d8fb37a6115138575a97e19881473de
sio:SIO_000628
miriam-gene:5444
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_provenance
{
dgn-np:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_assertion
dcterms:description
"[This study provides further evidence that genetic variation of the LT pathway, PON1, and CYP1A1 can modulate the atherogenic processes and eventually increase the risk of CAD in our study 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:25902778
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1280121.RAO__6PoqscWMVoKtGuBWv5sK1RwIzQ-QB3MuZ_fEq5YU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:26+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}