@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84
> .
@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:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_head
{
this:
np:hasAssertion
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_assertion
;
np:hasProvenance
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_provenance
;
np:hasPublicationInfo
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_assertion
a
np:Assertion
.
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_provenance
a
np:Provenance
.
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_assertion
{
miriam-gene:1535
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNe9304d73541694286965ffdcfa53f8de
sio:SIO_000628
miriam-gene:1535
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_provenance
{
dgn-np:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_assertion
dcterms:description
"[These results support the increased risk of developing early coronary artery disease and of having rapid progression of coronary stenosis in subjects carrying the C242T nucleotide transition among the Italian 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:16788250
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP134220.RA_R4eFd33GkB0EAh8O49U16zcMMxm3nihBark6WzoJ84130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:10+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" .
}