@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_head
{
this:
np:hasAssertion
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_assertion
;
np:hasProvenance
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_assertion
a
np:Assertion
.
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_provenance
a
np:Provenance
.
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_assertion
{
miriam-gene:5888
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGNaf593c0ec16f25301173839ed1b571d5
sio:SIO_000628
miriam-gene:5888
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_provenance
{
dgn-np:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_assertion
dcterms:description
"[We found that haplotypes in APEX1, BRCA2, ERCC2, and RAD51 were significantly associated with total ALL, while haplotypes in NBN and XRCC4, and CDKN2A were associated with structural and numerical change subtypes, respectively.]. 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:21987080
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP929960.RArNZWui7lzb6asz0pwX-rPJtUILLQLN2wvlMUjM8-XhE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:46+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}