@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ
> .
@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:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_head
{
this:
np:hasAssertion
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_assertion
;
np:hasProvenance
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_assertion
a
np:Assertion
.
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_provenance
a
np:Provenance
.
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_assertion
{
miriam-gene:4205
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN3c24353ec07828fa0c42a3643f8eb6ca
sio:SIO_000628
miriam-gene:4205
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_provenance
{
dgn-np:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_assertion
dcterms:description
"[Based on our data, we speculate that the CAG repeat polymorphism is associated with coronary heart disease in the Chinese population and the (CAG)(9) allele may be an independent predictive factor for CAD.]. 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:17579569
;
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:NP65676.RAPU8l3YIqgx8EONBfi8m_SNjj0ywNzjrNov167u7ZhzQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}