@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI
> .
@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:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_head
{
this:
np:hasAssertion
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_assertion
;
np:hasProvenance
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_provenance
;
np:hasPublicationInfo
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_assertion
a
np:Assertion
.
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_provenance
a
np:Provenance
.
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_assertion
{
miriam-gene:339345
a
ncit:C16612
.
lld:C1704272
a
ncit:C7057
.
dgn-gda:DGN5f171cdc5027b169eb5b113d99193972
sio:SIO_000628
miriam-gene:339345
,
lld:C1704272
;
a
sio:SIO_001121
.
}
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_provenance
{
dgn-np:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_assertion
dcterms:description
"[The inducible NOS (iNOS or NOS-2) is not detected in normal prostate, while it is expressed in the prostate of all benign prostatic hyperplasia (BPH) patients, even in the absence of prostatitis or systemic signs of an inflammatory condition.]. 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:10547579
;
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:NP489069.RAuNAw8ub6mtHt_NbTYxlwZc2APmmh1xBHWljNHcjelMI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}