@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4
> .
@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:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_head
{
this:
np:hasAssertion
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_assertion
;
np:hasProvenance
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_assertion
a
np:Assertion
.
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_provenance
a
np:Provenance
.
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_assertion
{
miriam-gene:7015
a
ncit:C16612
.
lld:C0034069
a
ncit:C7057
.
dgn-gda:DGNdfd6067bdc147df5fa19e29d0fefec1f
sio:SIO_000628
miriam-gene:7015
,
lld:C0034069
;
a
sio:SIO_001121
.
}
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_provenance
{
dgn-np:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_assertion
dcterms:description
"[Mutations in either of the two core components of telomerase, telomerase RNA (TR) or the catalytic protein component telomerase reverse transcriptase (TERT), cause the genetic disorders dyskeratosis congenita, pulmonary fibrosis, and other degenerative diseases.]. 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:21464209
;
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:NP156813.RA4vbVJ7YWx2nyF9gw7Ehe83--DnmQwJsPe84b_wwcNF4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}