@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA
> .
@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:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_head
{
this:
np:hasAssertion
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_assertion
;
np:hasProvenance
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_assertion
a
np:Assertion
.
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_provenance
a
np:Provenance
.
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_assertion
{
miriam-gene:3251
a
ncit:C16612
.
lld:C3469521
a
ncit:C7057
.
dgn-gda:DGNee986ce9b1d7f3f8d9cdfe85d94fe81b
sio:SIO_000628
miriam-gene:3251
,
lld:C3469521
;
a
sio:SIO_001121
.
}
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_provenance
{
dgn-np:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_assertion
dcterms:description
"[Knowing that the cellular events allowing the detection of mutations at the HPRT and the GPA locus differ, our results emphasize the possible correlation between events of spontaneous loss of heterozygosity and genetic predisposition to cancer as observed in FA.]. 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:7689157
;
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:NP1318368.RAXa4_7vRlSCCwJ8Qrby4gMvctqysvaLkKa6pwSUvx9PA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:44+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" .
}