@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o
> .
@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:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_head
{
this:
np:hasAssertion
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_assertion
;
np:hasProvenance
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_provenance
;
np:hasPublicationInfo
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_assertion
a
np:Assertion
.
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_provenance
a
np:Provenance
.
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_assertion
{
miriam-gene:3815
a
ncit:C16612
.
lld:C0521158
a
ncit:C7057
.
dgn-gda:DGNc6ed2d761673f37ca7d4231c886f8d4a
sio:SIO_000628
miriam-gene:3815
,
lld:C0521158
;
a
sio:SIO_001121
.
}
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_provenance
{
dgn-np:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_assertion
dcterms:description
"[Deletion of 48 base pairs of KIT exon 11, which preserved the reading frame, was identified in both primary and recurrent tumors, whereas deletion of one nucleotide of codon 642 of KIT exon 13, which changed the reading frame and induced a novel stop codon at amino acid 644, was found only in the recurrent tumor.]. 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:15543597
;
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:NP492614.RAqWfi1UjA8PN1oWU52TUhmNtyyysiDwAxyhZZpGHjc5o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}