@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4
> .
@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/v4.0.0/void/
> .
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_head
{
this:
np:hasAssertion
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_assertion
;
np:hasProvenance
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_assertion
a
np:Assertion
.
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_provenance
a
np:Provenance
.
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_assertion
{
miriam-gene:7486
a
ncit:C16612
.
lld:C1704436
a
ncit:C7057
.
dgn-gda:DGNdce99bcbc6bc17b7ea9a60b0412fd49e
sio:SIO_000628
miriam-gene:7486
,
lld:C1704436
;
a
sio:SIO_001121
.
}
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_provenance
{
dgn-np:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_assertion
dcterms:description
"[We report on a familial case of atypical Werner syndrome (a progeroid syndrome with Werner syndrome phenotype but without typical RECQL2 mutation) presenting with acute ischemic cerebral disease or peripheral artery disease associated with diffuse atherosclerosis, attributable to transmission of a novel LMNA mutation.]. 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:19095983
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP710194.RAyibO6_gPQPt_E8q0PwRFpgOldURHrROFK2fSAx_3kQ4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:07+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}