@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4
> .
@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:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_head
{
this:
np:hasAssertion
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_assertion
;
np:hasProvenance
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_provenance
;
np:hasPublicationInfo
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_assertion
a
np:Assertion
.
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_provenance
a
np:Provenance
.
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_assertion
{
miriam-gene:444
a
ncit:C16612
.
lld:C0598935
a
ncit:C7057
.
dgn-gda:DGN058ffd1b292ed938c6a69c16e9172a5d
sio:SIO_000628
miriam-gene:444
,
lld:C0598935
;
a
sio:SIO_001121
.
}
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_provenance
{
dgn-np:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_assertion
dcterms:description
"[High frequency and similar incidence of EGFR mutation in AAH, BAC, and ADC support that EGFR gene mutation occurs in the early stage of pulmonary ADC development and tumor initiation from the preneoplastic lung parenchyma to neoplastic conditions.]. 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:20512074
;
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:NP826118.RADCkBo5U2Gcx5JToWPefwhT4pk2hGKWteL64L1s5kes4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}