@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk
> .
@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:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_head
{
this:
np:hasAssertion
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_assertion
;
np:hasProvenance
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_provenance
;
np:hasPublicationInfo
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_assertion
a
np:Assertion
.
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_provenance
a
np:Provenance
.
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_assertion
{
miriam-gene:3425
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGNff7e53b98009968fb55e2304056dc239
sio:SIO_000628
miriam-gene:3425
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_provenance
{
dgn-np:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_assertion
dcterms:description
"[Patients with IDUA deficiency have a wide spectrum of disease ranging from an early onset, rapidly progressive form leading to death in the first decade of life, to an attenuated disease which manifests in adolescence and leads to progressive joint and cardiac disease but is associated with a normal life span.]. 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:15862278
;
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:NP293918.RAZ8UBlYP9o0-HaoONFw1OJKtNabT7-nYA0ojymb1XFlk130_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" .
}