@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q
> .
@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:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_head
{
this:
np:hasAssertion
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_assertion
;
np:hasProvenance
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_assertion
a
np:Assertion
.
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_provenance
a
np:Provenance
.
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C0265965
a
ncit:C7057
.
dgn-gda:DGN58ff3a04297130d056086e7cf197c62b
sio:SIO_000628
miriam-gene:2056
,
lld:C0265965
;
a
sio:SIO_001121
.
}
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_provenance
{
dgn-np:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_assertion
dcterms:description
"[Individuals in our families with mutated TERC did not have physical signs of dyskeratosis congenita, and their blood counts were nearly normal, but all had severely shortened telomeres, reduced haemopoietic function, and raised serum erythropoietin and thrombopoietin.]. 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:14630445
;
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:NP261744.RAh1Nrw3gkGoARvE5BIQtm0TBhZr3V1t4wrkXp4asw53Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}