@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY
> .
@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:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_head
{
this:
np:hasAssertion
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_assertion
;
np:hasProvenance
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_assertion
a
np:Assertion
.
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_provenance
a
np:Provenance
.
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C1704273
a
ncit:C7057
.
dgn-gda:DGN6b5d0f841366527b9f63393606e0e2c6
sio:SIO_000628
miriam-gene:4255
,
lld:C1704273
;
a
sio:SIO_001121
.
}
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_provenance
{
dgn-np:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_assertion
dcterms:description
"[Such mutations are frequently seen in the KRAS oncogene of large colorectal adenomas, but whether adenoma or mutational risk in humans is influenced by MGMT activity and alkylating agent exposure is unclear.]. 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:16891355
;
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:NP796082.RARAo14uGaO7sFsYt2TsmROZU7ZG1QV88lpQ3HNezdcUY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}