@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo
> .
@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:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_head
{
this:
np:hasAssertion
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_assertion
;
np:hasProvenance
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_provenance
;
np:hasPublicationInfo
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_assertion
a
np:Assertion
.
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_provenance
a
np:Provenance
.
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_assertion
{
miriam-gene:7376
a
ncit:C16612
.
lld:C0011156
a
ncit:C7057
.
dgn-gda:DGN7736679bcfb9273019a0cc8aa9c6507a
sio:SIO_000628
miriam-gene:7376
,
lld:C0011156
;
a
sio:SIO_001121
.
}
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_provenance
{
dgn-np:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_assertion
dcterms:description
"[Subsequently Xpa and Xpc knockouts have proved to be good models for the human NER deficiency disease, xeroderma pigmentosum, leading to speculation that the recombination, rather than the NER deficit is the key to the Ercc1 knockout phenotype.]. 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:12466203
;
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:NP709645.RASxYZ1jz2XFJ25LivFcjyW70Gz3Q4sSa1CVbECVFXduo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}