@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ
> .
@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:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_head
{
this:
np:hasAssertion
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_assertion
;
np:hasProvenance
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_assertion
a
np:Assertion
.
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_provenance
a
np:Provenance
.
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_assertion
{
miriam-gene:7376
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNf612df8e9d37e4c66ad13c3b820daa7e
sio:SIO_000628
miriam-gene:7376
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_provenance
{
dgn-np:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_assertion
dcterms:description
"[Deciphering the stepwise mechanism of NER has mostly relied on cells from rare patients presenting photosensitive, recessively inherited genetic disorders such as xeroderma pigmentosum (XP), trichothiodystrophy (TTD) and Cockayne (CS) syndromes.]. 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:18724052
;
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:NP308567.RAek1gdVoClrcTgpBnp2R7CytqZ9aYQlk46_dIIMCFCnQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}