@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI
> .
@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:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_head
{
this:
np:hasAssertion
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_assertion
;
np:hasProvenance
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_provenance
;
np:hasPublicationInfo
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_assertion
a
np:Assertion
.
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_provenance
a
np:Provenance
.
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C2732618
a
ncit:C7057
.
dgn-gda:DGNb91ea45f032192c4760c87c52fc47f5e
sio:SIO_000628
miriam-gene:3845
,
lld:C2732618
;
a
sio:SIO_001121
.
}
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_provenance
{
dgn-np:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_assertion
dcterms:description
"[Moreover, this alternate serrated pathway may itself also be quite biologically heterogeneous as reflected in sessile serrated adenomas (SSA) with virtually exclusive molecular signatures defined by the presence of either BRAF or KRAS mutations.]. 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:18567071
;
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:NP290455.RAJhhRxwWVNJulNtfTME0OLACWvgzGDqg637ufF-HSKpI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}