@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co
> .
@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:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_head
{
this:
np:hasAssertion
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_assertion
;
np:hasProvenance
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_provenance
;
np:hasPublicationInfo
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_assertion
a
np:Assertion
.
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_provenance
a
np:Provenance
.
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_assertion
{
miriam-gene:7054
a
ncit:C16612
.
lld:C0001546
a
ncit:C7057
.
dgn-gda:DGN8c3c3a097f20e2e9617b88a951fc933b
sio:SIO_000628
miriam-gene:7054
,
lld:C0001546
;
a
sio:SIO_001121
.
}
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_provenance
{
dgn-np:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_assertion
dcterms:description
"[A tetranucleotide repeat polymorphism in the first intron of the tyrosine hydroxylase (TH) gene, encoding a rate-limiting enzyme for the synthesis of catecholamines, is reported to have the potential to control expression of the gene and to be associated with suicidal behavior in patients with adjustment disorders.]. 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:17329957
;
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:NP507357.RAFrq7mVJYoVrGL98lJI7CnqFn1udqZF7pKVRVuhHN_co130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+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" .
}