@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE
> .
@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:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_head
{
this:
np:hasAssertion
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_assertion
;
np:hasProvenance
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_provenance
;
np:hasPublicationInfo
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_assertion
a
np:Assertion
.
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_provenance
a
np:Provenance
.
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_assertion
{
miriam-gene:55505
a
ncit:C16612
.
lld:C0265965
a
ncit:C7057
.
dgn-gda:DGN138e761f366f299a1cfea766d8fe8f44
sio:SIO_000628
miriam-gene:55505
,
lld:C0265965
;
a
sio:SIO_001121
.
}
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_provenance
{
dgn-np:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_assertion
dcterms:description
"[This further strengthens the model that defective telomere maintenance is the primary pathology in DC and substantiates the evidence in humans for the involvement of NOP10 in the telomerase complex and 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:17507419
;
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:NP381756.RAxqhX0_4i12YCwwrhER4ngoVH25E57Hx6dsNHhWePfdE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:45+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" .
}