@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E
> .
@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:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_head
{
this:
np:hasAssertion
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_assertion
;
np:hasProvenance
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_provenance
;
np:hasPublicationInfo
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_assertion
a
np:Assertion
.
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_provenance
a
np:Provenance
.
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0948089
a
ncit:C7057
.
dgn-gda:DGN171f919059548e08c6b8e77d8b0f34dd
sio:SIO_000628
miriam-gene:1543
,
lld:C0948089
;
a
sio:SIO_001121
.
}
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_provenance
{
dgn-np:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_assertion
dcterms:description
"[The results indicate that the homozygous CYP1A1 6235C genotype is associated with greater mortality following the onset of ACS, independent of ethnicity and clinical risk factors, but related to smoking history.]. 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:19650794
;
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:NP709694.RA72gQbh6L8RgtJ3V-OfwpQzjkY0haDEdpBjPHvyVqS8E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}