@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8
> .
@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:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_head
{
this:
np:hasAssertion
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_assertion
;
np:hasProvenance
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_provenance
;
np:hasPublicationInfo
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_assertion
a
np:Assertion
.
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_provenance
a
np:Provenance
.
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_assertion
{
miriam-gene:55135
a
ncit:C16612
.
lld:C0265965
a
ncit:C7057
.
dgn-gda:DGNe75e32d82d6f7ba7940252fca67f5708
sio:SIO_000628
miriam-gene:55135
,
lld:C0265965
;
a
sio:SIO_001121
.
}
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_provenance
{
dgn-np:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_assertion
dcterms:description
"[In iPSCs from a form of dyskeratosis congenita caused by mutations in TCAB1 (also known as WRAP53), telomerase catalytic activity is unperturbed, yet the ability of telomerase to lengthen telomeres is abrogated, because telomerase mislocalizes from Cajal bodies to nucleoli within the iPSCs.]. 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:21602826
;
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:NP780640.RAceAGyRPF2hf7HsmNiXpdec2An25EGZZ17u8m_Exizs8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}