@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_head
{
this:
np:hasAssertion
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_assertion
;
np:hasProvenance
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_provenance
;
np:hasPublicationInfo
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_assertion
a
np:Assertion
.
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_provenance
a
np:Provenance
.
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_assertion
{
miriam-gene:659
a
ncit:C16612
.
lld:C0019693
a
ncit:C7057
.
dgn-gda:DGN543ed326bacfa4cedb2d48247b560974
sio:SIO_000628
miriam-gene:659
,
lld:C0019693
;
a
sio:SIO_001121
.
}
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_provenance
{
dgn-np:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP415005.RARzFbDCr8NIokdDo28vytbcgHmFDcBp7WTRMLB3JKG8c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:53+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}