@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE
> .
@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:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_head
{
this:
np:hasAssertion
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_assertion
;
np:hasProvenance
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_provenance
;
np:hasPublicationInfo
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_assertion
a
np:Assertion
.
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_provenance
a
np:Provenance
.
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN568181d75b42239d9294cf1758b9bd95
sio:SIO_000628
miriam-gene:595
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_provenance
{
dgn-np:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_assertion
dcterms:description
"[Intratumoral gene expression levels of EGFR, VEGFR2 and NRP as well as polymorphisms in FCGR3A, CyclinD1 and EGFR could predict clinical outcome in mCRC patients enrolled in BOND2, independent of KRAS mutation status.]. 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:21036743
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47308.RAUecyVlezDABiIz4LeP5ajMszBfV7RjZQ24Gxm-J4nRE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}