@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU
> .
@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:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_head
{
this:
np:hasAssertion
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_assertion
;
np:hasProvenance
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_provenance
;
np:hasPublicationInfo
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_assertion
a
np:Assertion
.
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_provenance
a
np:Provenance
.
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_assertion
{
miriam-gene:7015
a
ncit:C16612
.
lld:C0034069
a
ncit:C7057
.
dgn-gda:DGNfefbacc87b087b0d67745fd281779442
sio:SIO_000628
miriam-gene:7015
,
lld:C0034069
;
a
sio:SIO_001121
.
}
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_provenance
{
dgn-np:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_assertion
dcterms:description
"[Some disease-linked TERT variants have altered properties of holoenzyme assembly or repeat addition processivity, but other TERT variants linked to either pulmonary fibrosis or hematopoietic deficiency retained normal hTR interaction and RNP catalytic activity.]. 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:20022961
;
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:NP633005.RAEX8YlF7tF7tDjXFcgPVsxj7mnRoTYnJAHfbH2lyz4nU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}