@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE
> .
@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/
> .
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_head
{
this:
np:hasAssertion
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_assertion
;
np:hasProvenance
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_provenance
;
np:hasPublicationInfo
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_assertion
a
np:Assertion
.
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_provenance
a
np:Provenance
.
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNaa28cfebe8428da4636790474c9fe52f
sio:SIO_000628
miriam-gene:1956
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_provenance
{
dgn-np:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_assertion
dcterms:description
"[Two types of somatic mutations (in-frame deletions and point substitutions) in the EGFR gene were successfully identified within 3.5h using this system, suggesting that this system could be used in clinical tests of EGFR gene mutations in lung cancer, and potentially other cancer, patients.]. 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:17187977
;
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:NP585927.RAq-h8T_n0QO0aQyYjUsi3djB8os_Lt53MQmhwU7G0agE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:10+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}