@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8
> .
@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:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_head
{
this:
np:hasAssertion
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_assertion
;
np:hasProvenance
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_provenance
;
np:hasPublicationInfo
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_assertion
a
np:Assertion
.
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_provenance
a
np:Provenance
.
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_assertion
{
miriam-gene:328
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN276340311e952ddfcc73fc6570fbb3a4
sio:SIO_000628
miriam-gene:328
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_provenance
{
dgn-np:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_assertion
dcterms:description
"[The previously reported association of the APEX Asp148Glu single nucleotide polymorphism (SNP) with cancer, and the suggestion of associations of the XRCC3 Thr241Met and hOGG1 Ser326Cys SNP sites with G(2) chromosomal radiosensitivity were investigated in a new study of 30 childhood and young adult cancer survivors, their 30 partners, and 55 offspring.]. 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:21113933
;
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:NP275034.RAyVyRCGS4dbCU1rNbK93Exr1rtvp_QR_iL8_e5766Ja8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}