@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE
> .
@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:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_head
{
this:
np:hasAssertion
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion
;
np:hasProvenance
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_provenance
;
np:hasPublicationInfo
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion
a
np:Assertion
.
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_provenance
a
np:Provenance
.
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion
{
miriam-gene:404672
a
ncit:C16612
.
lld:C0043346
a
ncit:C7057
.
dgn-gda:DGN676f276b874354248867e00fb19616ff
sio:SIO_000628
miriam-gene:404672
,
lld:C0043346
;
a
sio:SIO_001121
.
}
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_provenance
{
dgn-np:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion
dcterms:description
"[However, three further cell strains (TTD4VI and TTD6VI from two French siblings and TTD1BR from an English patient) showed restoration of normal UV-induced DNA repair synthesis after fusion with XP or TTD cells belonging to XP group D. These observations, which give the first indication that TTD is associated with repair defects behaving differently in the functional test of complementation, suggest some kind of causal connection between defective excision-repair factors and clinical features diagnostic for TTD.]. 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:8508495
;
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:NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}