@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE
> .
@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:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_head
{
this:
np:hasAssertion
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_assertion
;
np:hasProvenance
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_provenance
;
np:hasPublicationInfo
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_assertion
a
np:Assertion
.
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_provenance
a
np:Provenance
.
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_assertion
{
miriam-gene:5423
a
ncit:C16612
.
lld:C0043119
a
ncit:C7057
.
dgn-gda:DGNcf211275980eb9083c43b47a22deabd4
sio:SIO_000628
miriam-gene:5423
,
lld:C0043119
;
a
sio:SIO_001121
.
}
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_provenance
{
dgn-np:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_assertion
dcterms:description
"[One alternative splice DNA polymerase beta mRNA, generated by 87 nt deletion (exon 11) in the catalytic domain of this enzyme, was suggested to be responsible for genomic instability in tumorigenesis and in genetic disorder (Werner syndrome).]. 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:8900428
;
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:NP421541.RA2SBZpIyS2vKHASN1A6ByC_n2EKyroKGU2B-HL9ccMuE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+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" .
}