@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo
> .
@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:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_head
{
this:
np:hasAssertion
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_assertion
;
np:hasProvenance
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_provenance
;
np:hasPublicationInfo
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_assertion
a
np:Assertion
.
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_provenance
a
np:Provenance
.
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C1328247
a
ncit:C7057
.
dgn-gda:DGN114a576f0d2807f5ba6a078f04965b0c
sio:SIO_000628
miriam-gene:2056
,
lld:C1328247
;
a
sio:SIO_001121
.
}
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_provenance
{
dgn-np:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_assertion
dcterms:description
"[This model allows investigation of the impact of excessive erythrocytosis in individuals suffering from polycythemia vera, chronic mountain sickness, or in subjects tempted to abuse Epo by means of gene doping.]. 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:16690772
;
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:NP398739.RAnlKR0RDW422iMU29Hp1INv1HHFQsX5C6BXVjVQvApFo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:57+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" .
}