@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k
> .
@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:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_head
{
this:
np:hasAssertion
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_assertion
;
np:hasProvenance
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_provenance
;
np:hasPublicationInfo
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_assertion
a
np:Assertion
.
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_provenance
a
np:Provenance
.
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_assertion
{
miriam-gene:7294
a
ncit:C16612
.
lld:C1621958
a
ncit:C7057
.
dgn-gda:DGNb7af02e6ce1c3502215cbefdd63b2dd6
sio:SIO_000628
miriam-gene:7294
,
lld:C1621958
;
a
sio:SIO_001121
.
}
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_provenance
{
dgn-np:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_assertion
dcterms:description
"[Because the heterotopic-to-orthotopic transfer and propagation of glioblastoma multiforme preserves the receptor tyrosine kinase (RTK) gene amplification of patient tumors, this approach should facilitate investigations for determining the extent to which RTK amplification status influences tumor response to RTK-directed therapies.]. 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:15831234
;
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:NP825299.RAdwwXfzexRFlr2cI24WI2JNkFvZ4oypGt1S59zpOKo5k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}