@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y
> .
@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:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_head
{
this:
np:hasAssertion
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_assertion
;
np:hasProvenance
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_assertion
a
np:Assertion
.
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_provenance
a
np:Provenance
.
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN04b103482c56dc00d1c0c71417ade519
sio:SIO_000628
miriam-gene:1956
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_provenance
{
dgn-np:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_assertion
dcterms:description
"[The molecular understanding of this sequence has had a profound impact on our understanding of the process(s) of colonic carcinogenesis and this understanding has begun to change the clinical care of patients with colonic polyps and cancer including changes in therapy of established CRCs (anti-epidermal growth factor receptor antibody therapy is no longer offered to patients with mutant KRAS CRCs), identification of high-risk groups (diagnosis of Lynch syndrome by molecular analysis of CRCs) and the management of precursor lesions (identification of the serrated polyp pathway to CRC).]. 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:21266962
;
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:NP239086.RAjEsVDPFJlGljDqHJERrBYH9WngFeQoU0vxEs9c6xt8Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}