@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_head
{
this:
np:hasAssertion
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_assertion
;
np:hasProvenance
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_provenance
;
np:hasPublicationInfo
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_assertion
a
np:Assertion
.
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_provenance
a
np:Provenance
.
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_assertion
{
miriam-gene:7486
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN19cd0b4f8f1292a6c20607f31e75d560
sio:SIO_000628
miriam-gene:7486
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_provenance
{
dgn-np:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_assertion
dcterms:description
"[Deficiencies in genes encoding the RecQ helicases WRN and BLM lead to rare autosomal recessive diseases, Werner and Bloom syndromes, which have been implicated in early onset of aging, and predisposition to various types of cancer.]. 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:19945966
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP777902.RAuIjpW36m1izlWYmT4F_2VHBU4CFNGOPiqCDmGl52Qi4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:30+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}