@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8
> .
@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:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_head
{
this:
np:hasAssertion
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_assertion
;
np:hasProvenance
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_provenance
;
np:hasPublicationInfo
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_assertion
a
np:Assertion
.
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_provenance
a
np:Provenance
.
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_assertion
{
miriam-gene:221692
a
ncit:C16612
.
lld:C0342649
a
ncit:C7057
.
dgn-gda:DGNdd9ada1328db5a982a4ec846e0898929
sio:SIO_000628
miriam-gene:221692
,
lld:C0342649
;
a
sio:SIO_001122
.
}
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_provenance
{
dgn-np:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_assertion
dcterms:description
"[SNPs in the 9p21 and PHACTR1 gene loci were strongly associated with CAC and MI, and there are suggestive associations with both CAC and MI of SNPs in additional loci. Multiple genetic loci are associated with development of both underlying coronary atherosclerosis and clinical events.]. 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:22144573
;
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:NP96657.RAu4N2wpkp4X0MFUQT-pQ5WvPI8k4UyjQ0N9po9Fl36j8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:49+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" .
}