@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ
> .
@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:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_head
{
this:
np:hasAssertion
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_assertion
;
np:hasProvenance
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_assertion
a
np:Assertion
.
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_provenance
a
np:Provenance
.
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_assertion
{
miriam-gene:7298
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGNc17bc27c8f2c9b329dd90f17a175a370
sio:SIO_000628
miriam-gene:7298
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_provenance
{
dgn-np:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_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:NP980612.RAvkmQ7wZWdeHB00An3bkVF0Ks9BcNhZP3IBQM4fnGCdQ130_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" .
}