@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU
> .
@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:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_head
{
this:
np:hasAssertion
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_assertion
;
np:hasProvenance
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_provenance
;
np:hasPublicationInfo
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_assertion
a
np:Assertion
.
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_provenance
a
np:Provenance
.
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_assertion
{
miriam-gene:5644
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN5be0d695663639231981ae8b364a63d8
sio:SIO_000628
miriam-gene:5644
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_provenance
{
dgn-np:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_assertion
dcterms:description
"[Mutations in the cationic trypsinogen gene, pancreatic secretory trypsin inhibitor, and the cystic fibrosis conductance regulator gene do not account for the chronic pancreatitis noted in most patients with idiopathic chronic pancreatitis.]. 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:15506908
;
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:NP538315.RAOLIiGxE1hf05uZ-68OyaLdkEUIgSBsJkDW2rBL-liHU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}