@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ
> .
@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:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_head
{
this:
np:hasAssertion
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_assertion
;
np:hasProvenance
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_assertion
a
np:Assertion
.
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_provenance
a
np:Provenance
.
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_assertion
{
miriam-gene:7486
a
ncit:C16612
.
lld:C0009207
a
ncit:C7057
.
dgn-gda:DGN57a7334541994e0ef76f8ccc9a6094ee
sio:SIO_000628
miriam-gene:7486
,
lld:C0009207
;
a
sio:SIO_001121
.
}
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_provenance
{
dgn-np:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_assertion
dcterms:description
"[Werner syndrome (WS) is an autosomal recessive segmental progeroid syndrome caused by mutations in the Werner (WRN) gene leading to the early onset of many (but not all) aspects of normal aging.]. 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:16804003
;
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:NP600439.RAu2tUS9yhwJWlEzBcQYvNpr7NZTZzjC8N2NR4Rmd0SrQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}