@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0
> .
@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:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_head
{
this:
np:hasAssertion
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_assertion
;
np:hasProvenance
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_assertion
a
np:Assertion
.
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_provenance
a
np:Provenance
.
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_assertion
{
miriam-gene:238
a
ncit:C16612
.
lld:C0334121
a
ncit:C7057
.
dgn-gda:DGN8a25964bc0855c385e3c9874ba29edce
sio:SIO_000628
miriam-gene:238
,
lld:C0334121
;
a
sio:SIO_001121
.
}
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_provenance
{
dgn-np:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_assertion
dcterms:description
"[FISH evaluation of nine other IMTs identified CLTC as the fusion partner in one additional case, but RANBP2 was not involved in the remaining eight IMTs, suggesting that the variant partners involved in ALK rearrangements in IMTs are diverse.]. 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:17656252
;
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:NP382259.RA-Hd3aPWmQfhYzDr9BH7mml-LsoUnq6O6U-9shB0O4_0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:46+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" .
}