@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk
> .
@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:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_head
{
this:
np:hasAssertion
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_assertion
;
np:hasProvenance
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_provenance
;
np:hasPublicationInfo
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_assertion
a
np:Assertion
.
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_provenance
a
np:Provenance
.
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNcc1509c3a785cce0fb9779c59968b86d
sio:SIO_000628
miriam-gene:7515
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_provenance
{
dgn-np:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_assertion
dcterms:description
"[These data, using the classic skin carcinogenesis model, provide new insight on the role of the XRCC1 399 polymorphism in neoplasia and may help explain the conflicting results relating this polymorphism to cancer risk at various sites.]. 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:11782372
;
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:NP849042.RA9gER1xqZj-9u_4DdxiZjcTZZPB9uZ9Uq76t-waS71jk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}