@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro
> .
@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:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_head
{
this:
np:hasAssertion
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_assertion
;
np:hasProvenance
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_provenance
;
np:hasPublicationInfo
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_assertion
a
np:Assertion
.
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_provenance
a
np:Provenance
.
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_assertion
{
miriam-gene:4095
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGNa69a5b67e769c3e0d6798158fc94541c
sio:SIO_000628
miriam-gene:4095
,
lld:C0525045
;
a
sio:SIO_001121
.
}
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_provenance
{
dgn-np:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_assertion
dcterms:description
"[The findings of anticipation in this study of families with UPAD and previous findings in families with BPAD suggest that the variable expression of unstable expansions of trinucleotide repeats may turn out to be the basis of the continuum of liability in affective 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:8557885
;
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:NP701597.RACFY5dV6q4ECp1Ypzt0sfdSErLyCGlUOT8rG3kglG5Ro130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}