@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM
> .
@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:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_head
{
this:
np:hasAssertion
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_assertion
;
np:hasProvenance
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_provenance
;
np:hasPublicationInfo
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_assertion
a
np:Assertion
.
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_provenance
a
np:Provenance
.
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C1704272
a
ncit:C7057
.
dgn-gda:DGN750e90303a080a5c78366c8c295892d4
sio:SIO_000628
miriam-gene:5972
,
lld:C1704272
;
a
sio:SIO_001121
.
}
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_provenance
{
dgn-np:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_assertion
dcterms:description
"[Benign prostatic hyperplasia (BPH) is the most common hyperplastic disease in man and it is characterized by increased cellular growth (stromal and epithelial hyperplasia) and enhanced local sympathetic tone, both of which are known to be augmented by activation of the renin-angiotensin system (RAS) in other tissues.]. 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:11745693
;
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:NP782596.RAHE6QMQRbmPqIru5NENHzaW1p8qHUcOGhvHSyegWjQVM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}