@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk
> .
@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:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_head
{
this:
np:hasAssertion
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_assertion
;
np:hasProvenance
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_provenance
;
np:hasPublicationInfo
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_assertion
a
np:Assertion
.
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_provenance
a
np:Provenance
.
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN27d49fe654bd828e4e312fd0e216badd
sio:SIO_000628
miriam-gene:1636
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_provenance
{
dgn-np:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_assertion
dcterms:description
"[In studies where the underlying odds ratios are determined to be homogeneous, the overall odds ratios for myocardial infarction and coronary artery disease with regard to the ACE DD genotype are estimated using the Mantel-Haenszel method.]. 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:10554703
;
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:NP257821.RAFPLL0tBpKz1UnB0Ksv1Da-VzJu6xA7hlC_iewiDfYNk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+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" .
}