@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E
> .
@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:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_head
{
this:
np:hasAssertion
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_assertion
;
np:hasProvenance
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_provenance
;
np:hasPublicationInfo
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_assertion
a
np:Assertion
.
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_provenance
a
np:Provenance
.
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_assertion
{
miriam-gene:659
a
ncit:C16612
.
lld:C0018798
a
ncit:C7057
.
dgn-gda:DGNc8f2b0e54a8d4703662f4a899f6f0977
sio:SIO_000628
miriam-gene:659
,
lld:C0018798
;
a
sio:SIO_001121
.
}
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_provenance
{
dgn-np:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_assertion
dcterms:description
"[The aim of the present study was to determine if patients with both pulmonary arterial hypertension (PAH), due to pulmonary vascular obstructive disease, and congenital heart defects (CHD), have mutations in the gene encoding bone morphogenetic protein receptor (BMPR)-2.]. 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:15358693
;
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:NP890453.RAXDMpByUMyBaCQRDaBSyCBggmM-1FqnZqXZoOglZNE4E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:07+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" .
}