@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw
> .
@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:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_head
{
this:
np:hasAssertion
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_assertion
;
np:hasProvenance
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_assertion
a
np:Assertion
.
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_provenance
a
np:Provenance
.
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN15879c0bddaf41f96c8a28146b8351de
sio:SIO_000628
miriam-gene:1956
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_provenance
{
dgn-np:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_assertion
dcterms:description
"[These data, together with the nonoverlapping pattern of EGFR and BRAF mutations in human lung cancer, suggest that these lesions define distinct clinical entities whose treatment should be guided by prospective real-time genotyping.]. 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:19010912
;
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:NP703616.RAmbU7Y52eN9S7KmJwRyC0tYq47_x2LVkmRKTefRTKLFw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:04+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" .
}