@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0
> .
@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:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_head
{
this:
np:hasAssertion
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_assertion
;
np:hasProvenance
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_provenance
;
np:hasPublicationInfo
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_assertion
a
np:Assertion
.
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_provenance
a
np:Provenance
.
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_assertion
{
miriam-gene:57498
a
ncit:C16612
.
lld:C0152013
a
ncit:C7057
.
dgn-gda:DGN01a63724de97f4299d15625c5feaa99f
sio:SIO_000628
miriam-gene:57498
,
lld:C0152013
;
a
sio:SIO_001121
.
}
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_provenance
{
dgn-np:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_assertion
dcterms:description
"[Among the three methods for detecting EGFR mutations in plasma DNA samples of patients with advanced lung adenocarcinoma, direct gene sequencing had the lowest sensitivity, while Scorpion ARMS showed the highest mutation detecting capability.]. 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:21518597
;
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:NP295527.RACRAIZT6QoGKmFyKIq_32OxoEwRjON2EqokC-Fk-y2l0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}