@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w
> .
@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:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_head
{
this:
np:hasAssertion
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_assertion
;
np:hasProvenance
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_provenance
;
np:hasPublicationInfo
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_assertion
a
np:Assertion
.
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_provenance
a
np:Provenance
.
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN3b60759cf16d3a75499524c525168013
sio:SIO_000628
miriam-gene:3845
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_provenance
{
dgn-np:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_assertion
dcterms:description
"[Our findings indicate that the wild-type KRAS allele is occasionally lost in human lung cancer, and that the oncogenic activation of mutant KRAS is more frequently associated with an overexpression of the mutant allele than with a loss of the wild-type allele in human NSCLC development.]. 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:14601056
;
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:NP263118.RA3DFlQTBJE5EkCb2eL0yZwOR0RRyBHwCiWwtS0gx7c2w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}