@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg
> .
@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:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_head
{
this:
np:hasAssertion
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_assertion
;
np:hasProvenance
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_assertion
a
np:Assertion
.
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_provenance
a
np:Provenance
.
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0238198
a
ncit:C7057
.
dgn-gda:DGN7dcd05ac2ba3061e4496758b96834fb1
sio:SIO_000628
miriam-gene:1956
,
lld:C0238198
;
a
sio:SIO_001121
.
}
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_provenance
{
dgn-np:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_assertion
dcterms:description
"[The present case is not only of interest due to the rare coincidence of GIST and lung cancer, but also because there was an epidermal growth factor receptor gene mutation in the lung cancer and a c-kit mutation in the GIST.]. 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:22975558
;
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:NP789353.RAPYY-3GXBhquxwpvcGHKZ627Pmwpqi9gwW8dsUnhpsAg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:01+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" .
}