@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE
> .
@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:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_head
{
this:
np:hasAssertion
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_assertion
;
np:hasProvenance
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_provenance
;
np:hasPublicationInfo
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_assertion
a
np:Assertion
.
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_provenance
a
np:Provenance
.
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_assertion
{
miriam-gene:659
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN29b47a399c69d0bf8fbfdee7a0b94fca
sio:SIO_000628
miriam-gene:659
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_provenance
{
dgn-np:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_assertion
dcterms:description
"[BMPR2 was examined for mutations in 33 unrelated patients with sporadic PAH, and in two sisters with PAH, all of whom had taken fenfluramine derivatives, as well as in 130 normal controls.]. 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:12358323
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47805.RAHopNFvc3KktvKn1or9-apNxH3JhXDAL_5WoHv1R4qfE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}