@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8
> .
@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:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_head
{
this:
np:hasAssertion
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_assertion
;
np:hasProvenance
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_provenance
;
np:hasPublicationInfo
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_assertion
a
np:Assertion
.
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_provenance
a
np:Provenance
.
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN950f0c6bb540edd65a1dfe9e28d71e1e
sio:SIO_000628
miriam-gene:1956
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_provenance
{
dgn-np:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_assertion
dcterms:description
"[Mutations of epithelial growth factor receptor (EGFR) in exon 19 and 21 are both believed to be associated with carcinogenesis, sensitivity to tyrosine kinase drugs and with the prognosis of non-small cell lung cancers (NSCLCs).]. 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:21067269
;
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:NP162059.RAlS-1Wu4FkvDlqq-TfB74p-97L1GkHouaabS8MsVIsM8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}