@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M
> .
@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:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_head
{
this:
np:hasAssertion
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_assertion
;
np:hasProvenance
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_provenance
;
np:hasPublicationInfo
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_assertion
a
np:Assertion
.
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_provenance
a
np:Provenance
.
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_assertion
{
miriam-gene:238
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGN7bf94601711961f8acec552c90ca8331
sio:SIO_000628
miriam-gene:238
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_provenance
{
dgn-np:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_assertion
dcterms:description
"[The aberrant expression of full-length ALK receptor proteins has been reported in neuroblastomas and glioblastomas, while the occurrence of ALK fusion proteins in anaplastic large cell lymphoma (ALCL) has resulted in the identification of the new tumor entity, ALK-positive ALCL.]. 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:15583856
;
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:NP387238.RAeViHpWsSmKQ-wp15HPoEeAONDcB2NUP9HUXBVS-UH6M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:50+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" .
}