@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk
> .
@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:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_head
{
this:
np:hasAssertion
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_assertion
;
np:hasProvenance
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_provenance
;
np:hasPublicationInfo
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_assertion
a
np:Assertion
.
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_provenance
a
np:Provenance
.
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_assertion
{
miriam-gene:627
a
ncit:C16612
.
lld:C0812393
a
ncit:C7057
.
dgn-gda:DGNcf4d7f15878159680b66c572f37bea44
sio:SIO_000628
miriam-gene:627
,
lld:C0812393
;
a
sio:SIO_001121
.
}
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_provenance
{
dgn-np:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_assertion
dcterms:description
"[The polymorphism BDNF val66met of the brain derived neurotrophic factor (BDNF) is common, may increase the risk for depression, and affects BDNF secretion, critical for neuronal survival, plasticity, neurogenesis, and synaptic connectivity.]. 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:20346518
;
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:NP179173.RAqMX-lq4DFzDGdXuIQrgxym21WxBV-_FThm0_Fpr4Jfk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}