@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4
> .
@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:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_head
{
this:
np:hasAssertion
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_assertion
;
np:hasProvenance
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_provenance
;
np:hasPublicationInfo
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_assertion
a
np:Assertion
.
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_provenance
a
np:Provenance
.
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_assertion
{
miriam-gene:2056
a
ncit:C16612
.
lld:C0027022
a
ncit:C7057
.
dgn-gda:DGN3857d662afcdd86ae10257f0e0d07b8e
sio:SIO_000628
miriam-gene:2056
,
lld:C0027022
;
a
sio:SIO_001121
.
}
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_provenance
{
dgn-np:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_assertion
dcterms:description
"[Although none of these 10 cases have developed overt clinical and laboratory features of such a myeloproliferative disorder after a median observation period of two years, the presence of clonal karyotypic abnormalities in three cases, increased megakaryocyte colony growth in three cases and endogenous erythropoietin independent colony growth of the marrow erythroid progenitors in seven cases, argues strongly in favour of a primary haematological disorder.]. 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:2236481
;
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:NP534371.RAuze6TBnR2vTGeaLUI1AQkATXYlTOZszwuQ31J5YsDm4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}