@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI
> .
@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:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_head
{
this:
np:hasAssertion
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_assertion
;
np:hasProvenance
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_provenance
;
np:hasPublicationInfo
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_assertion
a
np:Assertion
.
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_provenance
a
np:Provenance
.
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_assertion
{
miriam-gene:497258
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN22f306f177572175eb43899cd0a744c3
sio:SIO_000628
miriam-gene:497258
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_provenance
{
dgn-np:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_assertion
dcterms:description
"[Two papers in this issue of Neuron show that reduced retrograde transport or signaling of the neurotrophins NGF or BDNF, respectively, may account for the neuronal pathology in mouse models of Down's syndrome.]. 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:16815323
;
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:NP616249.RAFcsE3CagkSk9yJEAwsfzNTjwrvN_XKhSMg3QUYAmAhI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}