@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY
> .
@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:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_head
{
this:
np:hasAssertion
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_assertion
;
np:hasProvenance
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_provenance
;
np:hasPublicationInfo
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_assertion
a
np:Assertion
.
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_provenance
a
np:Provenance
.
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_assertion
{
miriam-gene:9401
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGN05663038a56ef073b0ab894d80bf1fa4
sio:SIO_000628
miriam-gene:9401
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_provenance
{
dgn-np:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_assertion
dcterms:description
"[Mutations in three of the five known family members in humans, BLM, WRN and RECQL4, give rise to disorders that are characterized by predisposition to cancer and premature aging, emphasizing the importance of studying the RecQ proteins and their cellular activities.]. 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:17364146
;
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:NP293744.RA5BjbaJxGA6MXSMrgErN4icfp9VVSWCVAhSkixLAEihY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}