@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU
> .
@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:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_head
{
this:
np:hasAssertion
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_assertion
;
np:hasProvenance
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_provenance
;
np:hasPublicationInfo
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_assertion
a
np:Assertion
.
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_provenance
a
np:Provenance
.
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_assertion
{
miriam-gene:3981
a
ncit:C16612
.
lld:C0175691
a
ncit:C7057
.
dgn-gda:DGN8189b5eadc6e5cc36eda72c520ecb722
sio:SIO_000628
miriam-gene:3981
,
lld:C0175691
;
a
sio:SIO_001121
.
}
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_provenance
{
dgn-np:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_assertion
dcterms:description
"[Furthermore, expression of wild type DNA ligase IV completely complement the DNA repair defects in Dubowitz syndrome fibroblasts, suggesting that the DNA ligase IV mutation is solely responsible for the DNA repair defects.]. 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:23372718
;
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:NP400358.RAU4q8lNSLlE_AZFx1iKeQ0b0H7K-Pakc2Yue5k-zx7fU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}