@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI
> .
@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:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_head
{
this:
np:hasAssertion
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_assertion
;
np:hasProvenance
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_provenance
;
np:hasPublicationInfo
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_assertion
a
np:Assertion
.
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_provenance
a
np:Provenance
.
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_assertion
{
miriam-gene:2965
a
ncit:C16612
.
lld:C0043346
a
ncit:C7057
.
dgn-gda:DGNf9dc0121c478909cd9971ace7814bf57
sio:SIO_000628
miriam-gene:2965
,
lld:C0043346
;
a
sio:SIO_001121
.
}
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_provenance
{
dgn-np:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_assertion
dcterms:description
"[The involvement of some if not all of the TFIIH subunits in transcription and repair may explain the heterogeneity of the various and sometimes completely unrelated symptoms observed in xeroderma pigmentosum, Cockayne Syndrome and trichothiodystrophy disorders.]. 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:7980491
;
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:NP327094.RAfJtzmTPVEYtXObnpZil3Jw--L4lcHrHu0aSNgc6UTyI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}