@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns
> .
@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:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_head
{
this:
np:hasAssertion
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_assertion
;
np:hasProvenance
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_provenance
;
np:hasPublicationInfo
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_assertion
a
np:Assertion
.
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_provenance
a
np:Provenance
.
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_assertion
{
miriam-gene:2022
a
ncit:C16612
.
lld:C2973725
a
ncit:C7057
.
dgn-gda:DGNdec9878652aaee650cef5705c5eb8546
sio:SIO_000628
miriam-gene:2022
,
lld:C2973725
;
a
sio:SIO_001121
.
}
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_provenance
{
dgn-np:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_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
;
sio:SIO_000772
miriam-pubmed:23883380
;
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:NP519281.RAkEIYTjRKsOhsvX_MNVPciPuKiKxC5yv3a_3kaS12Vns130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:09+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" .
}