@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo
> .
@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:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_head
{
this:
np:hasAssertion
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_assertion
;
np:hasProvenance
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_provenance
;
np:hasPublicationInfo
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_assertion
a
np:Assertion
.
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_provenance
a
np:Provenance
.
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_assertion
{
miriam-gene:5644
a
ncit:C16612
.
lld:C0001339
a
ncit:C7057
.
dgn-gda:DGN6391a50c11babd0101d29751510ec751
sio:SIO_000628
miriam-gene:5644
,
lld:C0001339
;
a
sio:SIO_001121
.
}
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_provenance
{
dgn-np:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_assertion
dcterms:description
"[The etiology of acute pancreatitis (AP) seems to have changed during the last two decades, and since detection of mutations in the gene for cationic trypsinogen(PRSS1) causing hereditary pancreatitis some patients formerly diagnosed with idiopathic AP (IAP) turn out to have a genetic cause.]. 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:20720446
;
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:NP919545.RAyHen7vgiq9fNxfkzEADBcFFn8EK47C3tJIReBxHclUo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:24+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" .
}