@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_head
{
this:
np:hasAssertion
dgn-np:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_assertion
a
np:Assertion
.
dgn-np:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_provenance
a
np:Provenance
.
dgn-np:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4609
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN0fc3ee37752e19a1fa03a6ce507102e7
sio:SIO_000628
miriam-gene:4609
,
lld:C0376358
;
a
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.
}
dgn-np:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_provenance
{
dgn-np:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_assertion
dcterms:description
"[Although most amplified genomic regions tended to be large, amplifications at 8q24.21 were of particular interest because the affected regions are relatively small, are found in multiple cell lines, are located near MYC, an oncogene strongly implicated in prostate tumorigenesis, and are known to harbor SNPs that are associated with inherited susceptibility for prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:18670647
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP685383.RAsKqBikdeCFWdgjiLR6y0dXKXkGfuWe7PhFwAry0222k130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
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<
http://orcid.org/0000-0003-0169-8159
> ;
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"v4.0.0" .
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