@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY
> .
@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:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_head
{
this:
np:hasAssertion
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_assertion
;
np:hasProvenance
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_provenance
;
np:hasPublicationInfo
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_assertion
a
np:Assertion
.
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_provenance
a
np:Provenance
.
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_assertion
{
miriam-gene:627
a
ncit:C16612
.
lld:C0085281
a
ncit:C7057
.
dgn-gda:DGN8a07dffdaad4f9c379aaf72909e773f7
sio:SIO_000628
miriam-gene:627
,
lld:C0085281
;
a
sio:SIO_001121
.
}
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_provenance
{
dgn-np:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_assertion
dcterms:description
"[Potential roles for variants in the human BDNF gene in human brain disorders are supported by findings that include: (a) influences that this trophic factor can exert on important neurons, brain regions, and neurotransmitter systems, (b) changes in BDNF expression that follow altered neuronal activity and drug treatments, and (c) linkages or associations between genetic markers in or near BDNF and human traits and disorders that include depression, schizophrenia, addictions, and Parkinson's disease.]. 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:15666411
;
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:NP936399.RAmF6dwQXcyiBSYiYj5GJgThCbDjCCXMAQs_OnSQYrZTY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}