@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA
> .
@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:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_head
{
this:
np:hasAssertion
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_assertion
;
np:hasProvenance
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_provenance
;
np:hasPublicationInfo
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_assertion
a
np:Assertion
.
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_provenance
a
np:Provenance
.
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0235974
a
ncit:C7057
.
dgn-gda:DGN29dc246aacf3dbed009c4f6f0c688b54
sio:SIO_000628
miriam-gene:1029
,
lld:C0235974
;
a
sio:SIO_001121
.
}
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_provenance
{
dgn-np:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_assertion
dcterms:description
"[The molecular events involved in pancreatic cancer are becoming increasingly well characterized, with mutations in the dominant oncogene KRAS and the tumour suppressor genes TP53, CDKN2A and MADH4 being typically observed.]. 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:11169959
;
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:NP265973.RA7AHGt4wpj40UpWxU1FrqOYzRh4ciJzMbgxxJUWVftCA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}