@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc
> .
@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/v3.0.0/void/
> .
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_head
{
this:
np:hasAssertion
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_assertion
;
np:hasProvenance
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_provenance
;
np:hasPublicationInfo
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_assertion
a
np:Assertion
.
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_provenance
a
np:Provenance
.
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_assertion
{
miriam-gene:627
a
ncit:C16612
.
lld:C0036337
a
ncit:C7057
.
dgn-gda:DGNec85c70ec156dd4de43c442f01c9bf17
sio:SIO_000628
miriam-gene:627
,
lld:C0036337
;
a
sio:SIO_001122
.
}
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_provenance
{
dgn-np:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_assertion
dcterms:description
"[Individuals with schizoaffective disorder and other affective disorders were significantly more likely to carry two copies of the most common BDNF haplotype (containing the valine allele of the Val66Met polymorphism) compared with healthy volunteers.]. 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:19336781
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP266598.RAP-YgdDt9P_7QsOznPm6bPGTZ9M-YocoOxHRy6PLJ1Vc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:11+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}