@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog
> .
@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:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_head
{
this:
np:hasAssertion
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_assertion
;
np:hasProvenance
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_provenance
;
np:hasPublicationInfo
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_assertion
a
np:Assertion
.
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_provenance
a
np:Provenance
.
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0032584
a
ncit:C7057
.
dgn-gda:DGN53ce93092c0cde50f0e5ecaa8c04cc0c
sio:SIO_000628
miriam-gene:324
,
lld:C0032584
;
a
sio:SIO_001121
.
}
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_provenance
{
dgn-np:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_assertion
dcterms:description
"[Originating cells containing both short telomeres and APC mutations may give rise to polyps that exhibit short telomeres and are prone to telomere dysfunction, driving genomic instability and progression to malignancy.]. 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:23918447
;
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:NP401079.RAOFYUVL5Bq2WdKDWDz3C56rG3G5Xm2g47f-d-R7noYog130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}