@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok
> .
@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:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_head
{
this:
np:hasAssertion
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_assertion
;
np:hasProvenance
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_provenance
;
np:hasPublicationInfo
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_assertion
a
np:Assertion
.
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_provenance
a
np:Provenance
.
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGNda2b416ec62f7c05758739c766f6ccbb
sio:SIO_000628
miriam-gene:3845
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_provenance
{
dgn-np:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_assertion
dcterms:description
"[These data demonstrate that the RAS pathway signature is superior to KRAS mutation status for the prediction of dependence on RAS signaling, can predict response to PI3K and RAS pathway inhibitors, and is likely to have the most clinical utility in lung and breast tumors.]. 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:20591134
;
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:NP568167.RAu12VjrImPR57LBwxSlucZOAaHlg4n0Q8ApFd1BTMvok130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:42+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" .
}