@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA
> .
@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:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_head
{
this:
np:hasAssertion
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_assertion
;
np:hasProvenance
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_provenance
;
np:hasPublicationInfo
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_assertion
a
np:Assertion
.
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_provenance
a
np:Provenance
.
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_assertion
{
miriam-gene:627
a
ncit:C16612
.
lld:C0016667
a
ncit:C7057
.
dgn-gda:DGN0965d8fed55f8ff39fd1a0fdf27ea078
sio:SIO_000628
miriam-gene:627
,
lld:C0016667
;
a
sio:SIO_001121
.
}
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_provenance
{
dgn-np:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_assertion
dcterms:description
"[The Val66Met polymorphism in the BDNF gene may be involved in the alteration of normal secretion of the mature peptide and may modulate the epileptic phenotype observed in some patients with FXS.]. 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:21890420
;
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:NP634172.RAP6AvFUJ5OAMqDlJWxivgpLESly1DAnot0WYvLuHhblA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}