@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI
> .
@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:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_head
{
this:
np:hasAssertion
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_assertion
;
np:hasProvenance
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_provenance
;
np:hasPublicationInfo
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_assertion
a
np:Assertion
.
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_provenance
a
np:Provenance
.
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_assertion
{
miriam-gene:613
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN666ab0929bd480bec46ac919e01fac03
sio:SIO_000628
miriam-gene:613
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_provenance
{
dgn-np:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_assertion
dcterms:description
"[We report an elderly patient who presented with primary myelofibrosis (MF) with myeloid metaplasia (MMM), associated with idic(17)(p11.2) as the sole chromosomal abnormality, making this the first idic(17)(p11.2) myeloproliferative case reported in which the breakpoints are mapped to the breakpoint cluster region in proximal 17p.]. 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:16044457
;
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:NP393732.RAumoUVCZSvolJnxiXL5GK_R-NDgLFA0uURiCU4J_w3BI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}