@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8
> .
@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:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_head
{
this:
np:hasAssertion
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_assertion
;
np:hasProvenance
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_provenance
;
np:hasPublicationInfo
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_assertion
a
np:Assertion
.
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_provenance
a
np:Provenance
.
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_assertion
{
miriam-gene:9360
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN2933834534f684994462545bb5404c04
sio:SIO_000628
miriam-gene:9360
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_provenance
{
dgn-np:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_assertion
dcterms:description
"[Taking into account the mounting evidence about the role of cytochrome P450 (CYP) enzymes in cardiovascular physiology, CYP polymorphisms can be considered one of the major determinants of individual susceptibility to CVDs.]. 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:20093140
;
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:NP342099.RAgCq55UGNwetbEUt2b_enHgPCxpEW_1jCYJ6iF2poAT8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:21+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" .
}