@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY
> .
@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:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_head
{
this:
np:hasAssertion
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_assertion
;
np:hasProvenance
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_provenance
;
np:hasPublicationInfo
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_assertion
a
np:Assertion
.
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_provenance
a
np:Provenance
.
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_assertion
{
miriam-gene:1387
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN1d9419695f347acbde8e42aab3c208ee
sio:SIO_000628
miriam-gene:1387
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_provenance
{
dgn-np:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_assertion
dcterms:description
"[Although loss of RecQL4 function due to gene mutations causally linked to occurrence of human RTS with features of premature aging and cancer predisposition, our studies provide the evidence that overexpression of RecQL4 due to gene amplification play a critical role in human breast tumor progression.]. 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:23894508
;
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:NP290152.RAa09EHxQj3JcpJ5hqDbrQRASO0j9VWcTKnkOBjnx1THY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}