@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU
> .
@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:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_head
{
this:
np:hasAssertion
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_assertion
;
np:hasProvenance
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_provenance
;
np:hasPublicationInfo
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_assertion
a
np:Assertion
.
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_provenance
a
np:Provenance
.
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_assertion
{
miriam-gene:641
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGNbac6c505732e2a897787f952960491f9
sio:SIO_000628
miriam-gene:641
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_provenance
{
dgn-np:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_assertion
dcterms:description
"[Genetic defects in three of the five human RecQ helicases, BLM, WRN and RECQ4, give rise to defined syndromes associated with cancer predisposition, some features of premature ageing and chromosomal instability.]. 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:19657341
;
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:NP765399.RA0zVFWntaP3xoSzSy3A62rqy8DBtWHNzbeU_lduElgzU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}