@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI130_assertion
a
np:Assertion
.
dgn-np:NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI130_provenance
a
np:Provenance
.
dgn-np:NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2064
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN692397260097315f4972dc161c13cdc1
sio:SIO_000628
miriam-gene:2064
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI130_provenance
{
dgn-np:NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI130_assertion
dcterms:description
"[Here, we summarize the clinically relevant biomarker tests that should be considered in neurosurgical specimens based on the current recommendations of the European Society of Medical Oncology (ESMO) or the National Comprehensive Cancer Network (NCCN) for the most relevant primary tumor types: lung cancer (EGFR mutations, ALK rearrangement, BRAF mutations), breast cancer (HER2 amplification, steroid receptor overexpression), melanoma (BRAF mutations), and colorectal cancer (RAS mutations).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:25287912
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1226744.RAqAeLpyAaAjkTqzeRIt38AIZe8C3nbHpGcPY-F4vPQdI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:02+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
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;
pav:authoredBy
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> , <
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
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dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}