@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ
> .
@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:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_head
{
this:
np:hasAssertion
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_assertion
;
np:hasProvenance
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_assertion
a
np:Assertion
.
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_provenance
a
np:Provenance
.
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_assertion
{
miriam-gene:659
a
ncit:C16612
.
lld:C0020542
a
ncit:C7057
.
dgn-gda:DGN4a6f504606b557b56cccdd6e42a155ae
sio:SIO_000628
miriam-gene:659
,
lld:C0020542
;
a
sio:SIO_001121
.
}
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_provenance
{
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_assertion
dcterms:description
"[The increased incidence of the disease in young women, the familial cases, the association with autoimmune disorders, and the recent discovery that mutation of the PPH1 gene may not be restricted to familial PPH support the hypothesis that the development of pulmonary hypertension likely implies an individual susceptibility or predisposition, which is probably genetically determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:11590841
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP10113.RA0ZXScVfg1IqlBP6Pi0miz3G2uvvecOA5OoyBNK6TxZQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:02+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" .
}