@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k
> .
@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:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_head
{
this:
np:hasAssertion
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_assertion
;
np:hasProvenance
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_provenance
;
np:hasPublicationInfo
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_assertion
a
np:Assertion
.
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_provenance
a
np:Provenance
.
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_assertion
{
miriam-gene:6690
a
ncit:C16612
.
lld:C0238339
a
ncit:C7057
.
dgn-gda:DGNe9d6987c3582f5385059414dfd74fd32
sio:SIO_000628
miriam-gene:6690
,
lld:C0238339
;
a
sio:SIO_001121
.
}
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_provenance
{
dgn-np:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_assertion
dcterms:description
"[The coding regions of PRSS1 and SPINK1 genes were sequenced in 290 controls and 198 patients, of whom 120 were diagnosed as idiopathic (ICP), 41 as alcoholic (ACP), and 37 as hereditary pancreatitis (HP).]. 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:15082592
;
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:NP409292.RAkikj9oQ-1yZet2LS220sBNVlnoBhzvXcFzQTe7wzT0k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:03+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" .
}