@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io
> .
@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:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_head
{
this:
np:hasAssertion
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_assertion
;
np:hasProvenance
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_provenance
;
np:hasPublicationInfo
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_assertion
a
np:Assertion
.
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_provenance
a
np:Provenance
.
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_assertion
{
miriam-gene:7486
a
ncit:C16612
.
lld:C1306459
a
ncit:C7057
.
dgn-gda:DGN344cf12811a05faf2bf18a68f09ed56b
sio:SIO_000628
miriam-gene:7486
,
lld:C1306459
;
a
sio:SIO_001121
.
}
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_provenance
{
dgn-np:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_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:NP778032.RAitEodb6i3abGyI7YqFPPvSuho2xU20OiTvp5DwCj0io130_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" .
}