@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI
> .
@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:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_head
{
this:
np:hasAssertion
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_assertion
;
np:hasProvenance
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_provenance
;
np:hasPublicationInfo
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_assertion
a
np:Assertion
.
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_provenance
a
np:Provenance
.
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_assertion
{
miriam-gene:5156
a
ncit:C16612
.
lld:C1847319
a
ncit:C7057
.
dgn-gda:DGNdd936b9630fe7284f3d27cc246d2e6cb
sio:SIO_000628
miriam-gene:5156
,
lld:C1847319
;
a
sio:SIO_001121
.
}
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_provenance
{
dgn-np:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_assertion
dcterms:description
"[Given previous evidence that certain susceptibility loci and carcinogens are associated with characteristic mutations, or `signatures` in other cancers, we hypothesized that the characteristic somatic mutations in the KIT and PDGFRA genes in GIST tumors may similarly be mutational signatures that are causally linked to specific mutagens or susceptibility loci.]. 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:23637977
;
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:NP190044.RAPonSbpYKKoP1bUC0SauvC8RYerp5zWNYMhGRvCKiUxI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}