@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4
> .
@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:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_head
{
this:
np:hasAssertion
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_assertion
;
np:hasProvenance
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_provenance
;
np:hasPublicationInfo
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_assertion
a
np:Assertion
.
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_provenance
a
np:Provenance
.
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_assertion
{
miriam-gene:342977
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN13058795866211deb9f2ddd40ab3f6ca
sio:SIO_000628
miriam-gene:342977
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_provenance
{
dgn-np:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_assertion
dcterms:description
"[We studied two polymorphisms of the NOS3 gene, the VNTR in intron 4 (4VNTR) and the Glu298Asp polymorphism in exon 7, in relation to the existence of premature coronary artery disease and the occurrence of myocardial infarction.A total number of 370 individuals of the Greek population was examined by PCR-RFLP method.The patient group consisted of 209 subjects, aged less than 58 years presenting symptomatic coronary artery disease, documented by coronary angiography.]. 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:19014005
;
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:NP224196.RAMMRXZBH3oVIZhYDiPeF-zE6iROaaq0vt03xBssGeYf4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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" .
}