@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ
> .
@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:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_head
{
this:
np:hasAssertion
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_assertion
;
np:hasProvenance
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_assertion
a
np:Assertion
.
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_provenance
a
np:Provenance
.
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_assertion
{
miriam-gene:2993
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN7eaaf4bb6626206b30c742da6c592054
sio:SIO_000628
miriam-gene:2993
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_provenance
{
dgn-np:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_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-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:NP451244.RAqlZyYDtRaFpiTiDXF7hy5MC_qkspuAAygSbYntVmfTQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}