@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek
> .
@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:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_head
{
this:
np:hasAssertion
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_assertion
;
np:hasProvenance
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_provenance
;
np:hasPublicationInfo
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_assertion
a
np:Assertion
.
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_provenance
a
np:Provenance
.
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0887833
a
ncit:C7057
.
dgn-gda:DGNbc7781168b90d084cb05a4508e284a72
sio:SIO_000628
miriam-gene:1029
,
lld:C0887833
;
a
sio:SIO_001121
.
}
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_provenance
{
dgn-np:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_assertion
dcterms:description
"[Although the cytomorphologic features alone were not specific, the presence of a markedly elevated serum lipase level, cutaneous lesions of fat necrosis, and loss of heterozygosity at 1p, 5q25 at the APC locus, 9p21 at the p16 locus, and 17p13 at the p53 locus were essential in excluding the main differential diagnostic entities including pancreatic ductal carcinoma, pancreatic endocrine tumor, and pancreatoblastoma.]. 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:12112815
;
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:NP915869.RARKp-qxZL97fOjUCP5UjVlcuCF-2FHCAqilDMEgx9Xek130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}