@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ
> .
@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:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_head
{
this:
np:hasAssertion
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_assertion
;
np:hasProvenance
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_assertion
a
np:Assertion
.
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_provenance
a
np:Provenance
.
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C1318533
a
ncit:C7057
.
dgn-gda:DGNa53b40408653cd4aef6d9014df797aa9
sio:SIO_000628
miriam-gene:2056
,
lld:C1318533
;
a
sio:SIO_001121
.
}
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_provenance
{
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_assertion
dcterms:description
"[Absolute erythrocytoses are divided into primary, where the erythropoietic compartment is intrinsically abnormal, secondary, where the erythropoietic compartment is normal but is responding to external pathological events leading to an increased erythropoietin drive, and idiopathic, where neither a primary nor a secondary erythrocytosis can be established.]. 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:10640213
;
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:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:07+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" .
}