@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8
> .
@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:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_head
{
this:
np:hasAssertion
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_assertion
;
np:hasProvenance
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_provenance
;
np:hasPublicationInfo
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_assertion
a
np:Assertion
.
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_provenance
a
np:Provenance
.
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_assertion
{
miriam-gene:7466
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNf261f6a46d76d9c7f9fe25332b1c4613
sio:SIO_000628
miriam-gene:7466
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_provenance
{
dgn-np:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_assertion
dcterms:description
"[Mutation screening in patients with psychiatric disorders or diabetes mellitus has also been performed to test the hypothesis that heterozygous carriers of WFS1 gene mutations are at an increased risk following the observation that WS first-degree relatives have a higher frequency of these disorders.]. 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:11317350
;
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:NP315682.RA-ehYvyzvT0BFqmqgHx9nvEpifurYLndQAo1MQNXCrg8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:08+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" .
}