@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw
> .
@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:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_head
{
this:
np:hasAssertion
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_assertion
;
np:hasProvenance
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_provenance
;
np:hasPublicationInfo
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_assertion
a
np:Assertion
.
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_provenance
a
np:Provenance
.
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_assertion
{
miriam-gene:2071
a
ncit:C16612
.
lld:C0043346
a
ncit:C7057
.
dgn-gda:DGNc7f28a2c563acb5a168c46078b863d8c
sio:SIO_000628
miriam-gene:2071
,
lld:C0043346
;
a
sio:SIO_001121
.
}
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_provenance
{
dgn-np:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_assertion
dcterms:description
"[This integration resolves puzzles regarding XP helicase functions and suggests that XP helicase positions and activities within TFIIH detect and verify damage, select the damaged strand for incision, and coordinate repair with transcription and cell cycle through CAK signaling.]. 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:21571596
;
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:NP462876.RAlMTW52vo8q9CUv39KoetUFONXi6NNNymmfLSkvKl4Hw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}