@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM
> .
@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:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_head
{
this:
np:hasAssertion
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_assertion
;
np:hasProvenance
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_provenance
;
np:hasPublicationInfo
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_assertion
a
np:Assertion
.
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_provenance
a
np:Provenance
.
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0686377
a
ncit:C7057
.
dgn-gda:DGN202d2a5c245ad2f86bd1aca1a835b49e
sio:SIO_000628
miriam-gene:1956
,
lld:C0686377
;
a
sio:SIO_001121
.
}
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_provenance
{
dgn-np:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_assertion
dcterms:description
"[Further research is needed to distinguish between the underlying rates of developing CNS metastases between NSCLC with and without EGFR mutations and the impact of gefitinib and erlotinib versus chemotherapy on CNS failure patterns in these 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:21030498
;
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:NP184730.RAtZ09XcUZBnmf5S7NSqmxBhSeszefFJ0cBn48K2qDlXM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:40+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" .
}