@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ
> .
@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:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_head
{
this:
np:hasAssertion
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_assertion
;
np:hasProvenance
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_assertion
a
np:Assertion
.
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_provenance
a
np:Provenance
.
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0856281
a
ncit:C7057
.
dgn-gda:DGNcb0df45e5956ad136b1a9123207f9a58
sio:SIO_000628
miriam-gene:1080
,
lld:C0856281
;
a
sio:SIO_001121
.
}
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_provenance
{
dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_assertion
dcterms:description
"[In a population-based, well-defined group of patients first regarded as having pancreatitis of unknown origin (PUO), we identified, described, and compared the clinical and genetic aspects of patients with hereditary pancreatitis (HP) and with cystic fibrosis transmembrane conductance regulator gene (CFTR) and serine protease inhibitor Kazal type 1 gene (SPINK1) mutations with patients who retained the diagnosis of true idiopathic pancreatitis (tIP) after genetic testing for HP, SPINK1, and CFTR mutations.]. 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:20502448
;
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:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}