@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E
> .
@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:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_head
{
this:
np:hasAssertion
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_assertion
;
np:hasProvenance
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_provenance
;
np:hasPublicationInfo
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_assertion
a
np:Assertion
.
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_provenance
a
np:Provenance
.
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_assertion
{
miriam-gene:7376
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGNbcf57942861ec19008fcefdb7501ac52
sio:SIO_000628
miriam-gene:7376
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_provenance
{
dgn-np:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_assertion
dcterms:description
"[Defects in the DNA repair mechanism nucleotide excision repair (NER) may lead to tumors in xeroderma pigmentosum (XP) or to premature aging with loss of subcutaneous fat in Cockayne syndrome (CS).]. 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:20100872
;
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:NP594083.RAr7K5dwJmmK0lc-YA_HfiMzVVfpYvt5pnTpIAxOG4c4E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:57+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" .
}