@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ
> .
@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:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_head
{
this:
np:hasAssertion
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_assertion
;
np:hasProvenance
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_assertion
a
np:Assertion
.
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_provenance
a
np:Provenance
.
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_assertion
{
miriam-gene:4869
a
ncit:C16612
.
lld:C1516669
a
ncit:C7057
.
dgn-gda:DGN59d83db05ea204cfe0dbe20be6f93445
sio:SIO_000628
miriam-gene:4869
,
lld:C1516669
;
a
sio:SIO_001121
.
}
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_provenance
{
dgn-np:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_assertion
dcterms:description
"[Whether the rare expression of NPM/ALK is the result of clonal heterogeneity or an indication for clonal evolution and progression toward ALCL can only be answered by the repeated analysis of indicator cases during the course of the disease.]. 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:9209648
;
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:NP321066.RAmSKiXn0UZb2W5J3AgUL36nyFlcbh1ePrqPN0ljbCMDQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}