@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_head
{
this:
np:hasAssertion
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_assertion
;
np:hasProvenance
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_provenance
;
np:hasPublicationInfo
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_assertion
a
np:Assertion
.
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_provenance
a
np:Provenance
.
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_assertion
{
miriam-gene:238
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN6966136da185cf6473369d7ca20435ed
sio:SIO_000628
miriam-gene:238
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_provenance
{
dgn-np:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_assertion
dcterms:description
"[NSCLC specimens that harbored activating EGFR mutations were more likely to express low ERCC1 and TS mRNA levels, whereas patients with NSCLC who had ALK rearrangement were more likely to express low TS mRNA levels.]. 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:22569898
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP980607.RAvC_n5B3cClg9S9BaG4u32MtmoLZy4aTmOEPSwMnxfpA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:09+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}