@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU
> .
@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:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_head
{
this:
np:hasAssertion
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_assertion
;
np:hasProvenance
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_provenance
;
np:hasPublicationInfo
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_assertion
a
np:Assertion
.
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_provenance
a
np:Provenance
.
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_assertion
{
miriam-gene:5893
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN6132f5a457552fb41f3818836ebf02bf
sio:SIO_000628
miriam-gene:5893
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_provenance
{
dgn-np:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_assertion
dcterms:description
"[These data provide some evidence that variants in XRCC2 and LIG4 alter breast cancer risk, together with stronger evidence that variants of XRCC3 are associated with risk. If these results can be confirmed, understanding the functional basis should improve our understanding of the role of DNA repair in breast carcinogenesis.]. 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:12023982
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP52397.RA4qcQ94OjDhuWl9JtXSd-gF-wAkYvSPQbfVSWkl3yViU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}