@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk
> .
@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:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_head
{
this:
np:hasAssertion
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_assertion
;
np:hasProvenance
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_assertion
a
np:Assertion
.
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_provenance
a
np:Provenance
.
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_assertion
{
miriam-gene:1678
a
ncit:C16612
.
lld:C3469521
a
ncit:C7057
.
dgn-gda:DGNd073d2f6d1292eab08f4eb5f1e58d0b7
sio:SIO_000628
miriam-gene:1678
,
lld:C3469521
;
a
sio:SIO_001121
.
}
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_provenance
{
dgn-np:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_assertion
dcterms:description
"[Half of the extracts prepared showed normal levels of in vitro DNA repair synthesis in plasmids containing UV lesions, but the remainder of the extracts from the same cell lines showed deficient repair synthesis, suggesting the possibility of an unusually labile excision repair protein in XP-V. Fanconi's anemia (FA) cells show cellular hypersensitivity to cross-linking agents including cis-DDP.]. 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:2054778
;
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:NP850169.RA9RE9PkVRxpw78Tg14DH7CBEuNVo7TTGvxhvoC_UfcFk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:39+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" .
}