@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec
> .
@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:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_head
{
this:
np:hasAssertion
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_assertion
;
np:hasProvenance
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_provenance
;
np:hasPublicationInfo
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_assertion
a
np:Assertion
.
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_provenance
a
np:Provenance
.
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_assertion
{
miriam-gene:627
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN888573dc872fd009d048bc45de5cd03e
sio:SIO_000628
miriam-gene:627
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_provenance
{
dgn-np:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_assertion
dcterms:description
"[BDNF has emerged as one of the most important signaling molecules for the developing nervous system as well as the impaired nervous system, and multiple diseases, such as Alzheimer's, Parkinson's, Huntington's, epilepsy, Rett's syndrome, and psychiatric depression, are linked by their association with potential dysregulation of BDNF-driven signal transduction programs.]. 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:18208542
;
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:NP211149.RAdpxHEIVzjw15IYGYKK0RN-v-wi5DuF8OFSaicnte1ec130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:56+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" .
}