@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE
> .
@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:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_head
{
this:
np:hasAssertion
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_assertion
;
np:hasProvenance
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_provenance
;
np:hasPublicationInfo
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_assertion
a
np:Assertion
.
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_provenance
a
np:Provenance
.
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0009207
a
ncit:C7057
.
dgn-gda:DGNa75f1bf64afea3bbde158f3173b78c21
sio:SIO_000628
miriam-gene:2068
,
lld:C0009207
;
a
sio:SIO_001122
.
}
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_provenance
{
dgn-np:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_assertion
dcterms:description
"[suggest a model of how DNA is bound to the XPD protein, and can rationalize several of the mutations in the human XPD gene that lead to one of three severe diseases, xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy ]. 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:18578568
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP152899.RAmI5DLqbK7ZEi8GH80nHwPLSA-N3ITVszd_Wfb3tg9eE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:21+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" .
}