@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_head
{
this:
np:hasAssertion
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion
;
np:hasProvenance
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion
a
np:Assertion
.
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance
a
np:Provenance
.
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C1955934
a
ncit:C7057
.
dgn-gda:DGN3a09da0e8460260ace83713043c833a3
sio:SIO_000628
miriam-gene:2068
,
lld:C1955934
;
a
sio:SIO_001121
.
}
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_provenance
{
dgn-np:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_assertion
dcterms:description
"[These results establish the essential function of the XPD protein in mammals and in cellular viability and are consistent with the notion that only subtle XPD mutations are found in XP, XP/Cockayne syndrome, and trichothiodystrophy patients.]. 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:9426063
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1386737.RAH8R_vfwJ-1ZpE5TNtqiAHQlTmyMmq0nKJZ7uLUTLTVQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:14+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}