@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw
> .
@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:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_head
{
this:
np:hasAssertion
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_assertion
;
np:hasProvenance
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_assertion
a
np:Assertion
.
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_provenance
a
np:Provenance
.
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_assertion
{
miriam-gene:79017
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN547b7376fb8e34e3bb8ceeb9951d69d1
sio:SIO_000628
miriam-gene:79017
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_provenance
{
dgn-np:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_assertion
dcterms:description
"[This review analyzes the available data regarding variation of the CAG and GGC repeat sequences among different racial and ethnic populations, and the implications of these variations for prostate cancer risk.]. 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:12084187
;
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:NP484544.RAjSFhtALBdgyTQJinjpUaJj9N3Y1xQ69cOmWEt4R4lqw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}