@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw
> .
@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:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_head
{
this:
np:hasAssertion
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_assertion
;
np:hasProvenance
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_provenance
;
np:hasPublicationInfo
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_assertion
a
np:Assertion
.
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_provenance
a
np:Provenance
.
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0002965
a
ncit:C7057
.
dgn-gda:DGN77a94bbb2c638bb2d9895d9da2d4996b
sio:SIO_000628
miriam-gene:1636
,
lld:C0002965
;
a
sio:SIO_001121
.
}
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_provenance
{
dgn-np:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_assertion
dcterms:description
"[The present study was performed to investigate the correlation between ACE genetic polymorphism and acute coronary syndrome by comparing the distribution of ACE genotypes and ACE activities in patients with acute MI and unstable angina with those in control group.]. 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:9364295
;
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:NP220218.RAuc2_QESnVT4XAO1GvYOOXNnYW0O55XSrhCxJ-uthmPw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}