@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU
> .
@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:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_head
{
this:
np:hasAssertion
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_assertion
;
np:hasProvenance
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_provenance
;
np:hasPublicationInfo
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_assertion
a
np:Assertion
.
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_provenance
a
np:Provenance
.
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_assertion
{
miriam-gene:1736
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGNaeeed227fdd65fbbe7f6fd70877e1993
sio:SIO_000628
miriam-gene:1736
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_provenance
{
dgn-np:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_assertion
dcterms:description
"[These findings demonstrate the importance of telomerase in humans and highlight how its deficiency (through DKC1 and TERC mutations) results in multiple abnormalities including premature ageing, bone marrow failure and cancer.]. 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:15613268
;
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:NP320656.RAOhh56GeDzAgViC8EmOp-plk383utvPPXuDGg2W729EU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}