@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g
> .
@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:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_head
{
this:
np:hasAssertion
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_assertion
;
np:hasProvenance
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_assertion
a
np:Assertion
.
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_provenance
a
np:Provenance
.
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_assertion
{
miriam-gene:4824
a
ncit:C16612
.
lld:C0282612
a
ncit:C7057
.
dgn-gda:DGNa20e5ad41ee81d534920e8ea5fe5723c
sio:SIO_000628
miriam-gene:4824
,
lld:C0282612
;
a
sio:SIO_001121
.
}
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_provenance
{
dgn-np:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_assertion
dcterms:description
"[Therefore, whereas genetic disruption of NKX3.1 in mice leads to PIN, nongenetic mechanisms reduce NKX3.1 protein levels early in human prostate carcinogenesis, which may facilitate both proliferation and DNA damage in atrophic and PIN cells.]. 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:17108105
;
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:NP722263.RAMTOthSzTBuIuKyM-_KQnrxhRFAi85iAcDw8ou23iP_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}