@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo
> .
@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:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_head
{
this:
np:hasAssertion
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_assertion
;
np:hasProvenance
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_provenance
;
np:hasPublicationInfo
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_assertion
a
np:Assertion
.
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_provenance
a
np:Provenance
.
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_assertion
{
miriam-gene:7517
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN5a65bdf15f541c08ac96da4e9c6d0df7
sio:SIO_000628
miriam-gene:7517
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_provenance
{
dgn-np:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_assertion
dcterms:description
"[Polymorphisms have been identified in several DNA repair genes, such as XRCC1, XPD, XRCC3, and RAD51, but the influence of specific genetic variants on repair phenotype and cancer risk has not yet been clarified.]. 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:16475125
;
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:NP528749.RAaUYYhQPJcUiw-MRgOAOu9oqDLd3CZCncHNqPECA8pyo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:19+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" .
}