@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek
> .
@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/v3.0.0/void/
> .
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_head
{
this:
np:hasAssertion
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_assertion
;
np:hasProvenance
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_provenance
;
np:hasPublicationInfo
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_assertion
a
np:Assertion
.
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_provenance
a
np:Provenance
.
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_assertion
{
miriam-gene:26277
a
ncit:C16612
.
lld:C2986691
a
ncit:C7057
.
dgn-gda:DGN5a57da1eb81a19fbedd4a9a88a3385d8
sio:SIO_000628
miriam-gene:26277
,
lld:C2986691
;
a
sio:SIO_001121
.
}
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_provenance
{
dgn-np:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_assertion
dcterms:description
"[Remarkably, the PTVML HP1-binding site is embedded in the recently identified cluster of mutations in TIN2 that gives rise to dyskeratosis congenita (DC), an inherited bone marrow failure syndrome caused by defects in telomere maintenance.]. 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:21865325
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP882857.RARqgiT5jRdB_ubfDvH5nQPMG9kEka9mVAiWWPokEI_Ek130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:38+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}