@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc
> .
@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:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_head
{
this:
np:hasAssertion
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_assertion
;
np:hasProvenance
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_provenance
;
np:hasPublicationInfo
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_assertion
a
np:Assertion
.
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_provenance
a
np:Provenance
.
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN51fbe3691e3faffd4fc58ef8503f44dc
sio:SIO_000628
miriam-gene:3918
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_provenance
{
dgn-np:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_assertion
dcterms:description
"[Polymerase chain reaction detection of epithelial growth factor receptor (EGFR) mutations in cerebrospinal fluid (CSF), which are predictive markers for EGFR tyrosine kinase inhibitor therapy in lung cancer, might be important to diagnose and to treat NM in patients with lung cancer.]. 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:21610522
;
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:NP778469.RAy4y6LmOGOSg92SRRvf1fb74dCjSYTT5A7O6S_lkQQSc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}