@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE
> .
@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:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_head
{
this:
np:hasAssertion
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_assertion
;
np:hasProvenance
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_provenance
;
np:hasPublicationInfo
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_assertion
a
np:Assertion
.
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_provenance
a
np:Provenance
.
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_assertion
{
miriam-gene:659
a
ncit:C16612
.
lld:C0009782
a
ncit:C7057
.
dgn-gda:DGN20890bd30dae87b7090afb7c19afd059
sio:SIO_000628
miriam-gene:659
,
lld:C0009782
;
a
sio:SIO_001121
.
}
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_provenance
{
dgn-np:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_assertion
dcterms:description
"[The causes in cases without a BMPR2 mutation are unknown, but a syndrome of pulmonary arterial hypertension (PAH) similar to hereditary PPH is associated with systemic connective tissue disease, congenital heart disease, portal hypertension, and human immunodeficiency virus infection, or with the use of appetite-suppressant drugs.]. 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:14516151
;
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:NP862803.RAaSfyONdaUA5bOx4Hw09VfV_LeFbALmaI1uzTC_SttNE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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" .
}