@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0
> .
@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:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_head
{
this:
np:hasAssertion
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_assertion
;
np:hasProvenance
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_provenance
;
np:hasPublicationInfo
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_assertion
a
np:Assertion
.
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_provenance
a
np:Provenance
.
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_assertion
{
miriam-gene:7239
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNf42246f9c058c6c6dc0333443d33752e
sio:SIO_000628
miriam-gene:7239
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_provenance
{
dgn-np:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_assertion
dcterms:description
"[Asthma history, frequent pain, and higher values for TRV and WBC count were independently associated with history of acute pulmonary events in hemoglobin SS patients and frequent pain was associated in those with other genotypes.]. 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:23560516
;
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:NP632852.RAfsaXX9NVAPGAQOxDLAFNR1WjFPH9e7Pbu4-5eXeG-E0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}