@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY
> .
@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:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_head
{
this:
np:hasAssertion
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_assertion
;
np:hasProvenance
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_provenance
;
np:hasPublicationInfo
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_assertion
a
np:Assertion
.
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_provenance
a
np:Provenance
.
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_assertion
{
miriam-gene:57126
a
ncit:C16612
.
lld:C0040028
a
ncit:C7057
.
dgn-gda:DGNea4ea7747d5c3130259e7730c2ae67c3
sio:SIO_000628
miriam-gene:57126
,
lld:C0040028
;
a
sio:SIO_001121
.
}
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_provenance
{
dgn-np:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_assertion
dcterms:description
"[The question arises whether this mutation is observed in those patients with ET and IMF who have also displayed previously described molecular markers, notably the ability to form endogenous erythroid colonies (EECs), overexpression of polycythemia rubra vera 1 (PRV-1), and decreased c-Mpl expression.]. 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:15985544
;
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:NP570386.RAt2pZ8KyPJNE5YLS8ZOeIaFgMVLjg35LDWVnNBrqbCfY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}