@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po130_assertion
a
np:Assertion
.
dgn-np:NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po130_provenance
a
np:Provenance
.
dgn-np:NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2022
a
ncit:C16612
.
lld:C3714844
a
ncit:C7057
.
dgn-gda:DGN9fa17e10ea7cb1c6360f0182ea0d1c65
sio:SIO_000628
miriam-gene:2022
,
lld:C3714844
;
a
sio:SIO_001121
.
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dgn-np:NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po130_provenance
{
dgn-np:NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po130_assertion
dcterms:description
"[We studied a family in which multiple members had pulmonary arterial hypertension without identifiable mutations in any of the genes known to be associated with the disease, including BMPR2, ALK1, ENG, SMAD9, and CAV1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:23883380
;
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 .
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dgn-np:NP1096425.RACxoxS8aJcpuwZM24ZNRSJyqH56mLkU6zGWndQVMe7Po130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:03+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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
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"v4.0.0" .
}