@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y
> .
@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:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_head
{
this:
np:hasAssertion
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_assertion
;
np:hasProvenance
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_assertion
a
np:Assertion
.
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_provenance
a
np:Provenance
.
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_assertion
{
miriam-gene:5277
a
ncit:C16612
.
lld:C0002878
a
ncit:C7057
.
dgn-gda:DGN16cd40a435bc52bae95bad7564d374a5
sio:SIO_000628
miriam-gene:5277
,
lld:C0002878
;
a
sio:SIO_001121
.
}
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_provenance
{
dgn-np:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_assertion
dcterms:description
"[The development of pulmonary arterial hypertension (PAH) is the leading cause of mortality in patients with thalassemia and sickle cell anemia and was reported to occur in hemolytic anemias such as hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria.]. 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:17356397
;
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:NP326882.RA1dB_PyRPmioByszhz_9PZgEzhHKQlRufp5e6jEaeq2Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}