@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E
> .
@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:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_head
{
this:
np:hasAssertion
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_assertion
;
np:hasProvenance
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_provenance
;
np:hasPublicationInfo
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_assertion
a
np:Assertion
.
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_provenance
a
np:Provenance
.
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_assertion
{
miriam-gene:5592
a
ncit:C16612
.
lld:C0027022
a
ncit:C7057
.
dgn-gda:DGN1838e57b2869a188a3a9b93640aa5c36
sio:SIO_000628
miriam-gene:5592
,
lld:C0027022
;
a
sio:SIO_001121
.
}
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_provenance
{
dgn-np:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_assertion
dcterms:description
"[X-chromosome DNA probes for the phosphoglycerate kinase (PGK) and hypoxanthine phosphoribosyl transferase (HPRT) genes were used to study clonality in haemopoietic cells from 63 women with myeloproliferative disease, idiopathic erythrocytosis, secondary erythrocytosis or normal red cell volumes.]. 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:2775657
;
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:NP230426.RAVaIGjPhNP4UqPlHzvAfYyUv6BjnMclfx2utIG9vbu9E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}