@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY
> .
@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:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_head
{
this:
np:hasAssertion
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_assertion
;
np:hasProvenance
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_provenance
;
np:hasPublicationInfo
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_assertion
a
np:Assertion
.
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_provenance
a
np:Provenance
.
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_assertion
{
miriam-gene:7517
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN9a62cb81b0bc0ee2c8609c8f5796c64c
sio:SIO_000628
miriam-gene:7517
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_provenance
{
dgn-np:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_assertion
dcterms:description
"[We observed that the XRCC3 18085T (241Met) allele and its associated haplotype were significantly inversely associated with the risks of SCC and BCC, whereas the XRCC3 4552C allele along with its associated haplotype and the XRCC2 30833A allele were significantly associated with increased BCC 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:15126335
;
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:NP315894.RADxxCHDUeLc0ZF4sOJV52aP67CkvkOcqna7eeQnJCTfY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}