@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I
> .
@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:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_head
{
this:
np:hasAssertion
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_assertion
;
np:hasProvenance
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_provenance
;
np:hasPublicationInfo
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_assertion
a
np:Assertion
.
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_provenance
a
np:Provenance
.
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_assertion
{
miriam-gene:113451
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN6e10885be9c127d8ce4d06a25979333a
sio:SIO_000628
miriam-gene:113451
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_provenance
{
dgn-np:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_assertion
dcterms:description
"[These results suggest that mutations are good markers of different aetiologies and histopathological forms of lung cancers but have little prognostic value, with the exception of KRAS mutation, which may have a prognostic value in ADC.]. 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:22267755
;
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:NP382057.RAdB4obYaYkJljcUNasgMNtHjyOka6UlNhdYwm1ZHNU2I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:46+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" .
}