@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0
> .
@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:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_head
{
this:
np:hasAssertion
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_assertion
;
np:hasProvenance
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_provenance
;
np:hasPublicationInfo
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_assertion
a
np:Assertion
.
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_provenance
a
np:Provenance
.
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGNccb23041709b2b6b178d376cc83c5b9d
sio:SIO_000628
miriam-gene:1636
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_provenance
{
dgn-np:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_assertion
dcterms:description
"[Insertion/deletion (I/D) polymorphisms in intron 16 of the angiotensin converting enzyme gene (ACE) are associated with the plasma angiotensin converting enzyme (ACE) levels, and individuals with the DD allele have been reported to be more susceptible to cardiovascular disease than those without.]. 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:12733698
;
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:NP238797.RAIRtDh6Z7Mc49xBJM163h9AAY-auRvJ6RBS8PjQv9nz0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}