@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE
> .
@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:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_head
{
this:
np:hasAssertion
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_assertion
;
np:hasProvenance
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_provenance
;
np:hasPublicationInfo
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_assertion
a
np:Assertion
.
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_provenance
a
np:Provenance
.
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_assertion
{
miriam-gene:6690
a
ncit:C16612
.
lld:C0271642
a
ncit:C7057
.
dgn-gda:DGN653ca3c39743e9b1fcea537f7b8c3cc3
sio:SIO_000628
miriam-gene:6690
,
lld:C0271642
;
a
sio:SIO_001121
.
}
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_provenance
{
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_assertion
dcterms:description
"[Since SPINK1 mutations in Europeans and North Americans are associated with idiopathic chronic pancreatitis that is phenotypically different from FCPD, we further conclude that mutated SPINK1 markedly increases the risk of developing a variety of pancreatic diseases possibly through a chronic elevation of active trypsin within the pancreas.]. 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:12120202
;
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:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}