@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI
> .
@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:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_head
{
this:
np:hasAssertion
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_assertion
;
np:hasProvenance
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_provenance
;
np:hasPublicationInfo
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_assertion
a
np:Assertion
.
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_provenance
a
np:Provenance
.
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_assertion
{
miriam-gene:83886
a
ncit:C16612
.
lld:C0085669
a
ncit:C7057
.
dgn-gda:DGNe9b60752a519746fb6f687896eb6097a
sio:SIO_000628
miriam-gene:83886
,
lld:C0085669
;
a
sio:SIO_001121
.
}
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_provenance
{
dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_assertion
dcterms:description
"[Although previous candidate genetic studies have identified mutations in MPN patients who develop acute leukemia, the complement of genetic abnormalities in MPN patients who undergo LT is not known nor have specific molecular abnormalities been shown to have clinical relevance in this setting.]. 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:22431577
;
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:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}