@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg
> .
@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:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_head
{
this:
np:hasAssertion
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_assertion
;
np:hasProvenance
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_provenance
;
np:hasPublicationInfo
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_assertion
a
np:Assertion
.
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_provenance
a
np:Provenance
.
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_assertion
{
miriam-gene:1621
a
ncit:C16612
.
lld:C0026267
a
ncit:C7057
.
dgn-gda:DGN65b726fec6074b7f55568e7eb29a5866
sio:SIO_000628
miriam-gene:1621
,
lld:C0026267
;
a
sio:SIO_001121
.
}
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_provenance
{
dgn-np:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_assertion
dcterms:description
"[The finding of genetic mutations responsible for DBH deficiency and orthostatic intolerance leads us to believe that genetic causes of other autonomic disorders will be found, enabling us to design more effective therapeutic interventions.]. 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:12438171
;
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:NP664442.RA-kOFnW3M6VSthqDu1Q2KjIEkb-D3T9fFuFxUxoU6fJg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:41+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" .
}