@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM
> .
@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:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_head
{
this:
np:hasAssertion
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_assertion
;
np:hasProvenance
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_provenance
;
np:hasPublicationInfo
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_assertion
a
np:Assertion
.
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_provenance
a
np:Provenance
.
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_assertion
{
miriam-gene:238
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN58836661e53c0f64b440e6d1f46dc84b
sio:SIO_000628
miriam-gene:238
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_provenance
{
dgn-np:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_assertion
dcterms:description
"[The major recommendations are to use testing for EGFR mutations and ALK fusions to guide patient selection for therapy with an epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) inhibitor, respectively, in all patients with advanced-stage adenocarcinoma, regardless of sex, race, smoking history, or other clinical risk factors, and to prioritize EGFR and ALK testing over other molecular predictive tests.]. 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:23562183
;
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:NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}