@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_head
{
this:
np:hasAssertion
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_assertion
;
np:hasProvenance
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_provenance
;
np:hasPublicationInfo
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_assertion
a
np:Assertion
.
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_provenance
a
np:Provenance
.
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_assertion
{
miriam-gene:6690
a
ncit:C16612
.
lld:C0149521
a
ncit:C7057
.
dgn-gda:DGN6b63f0ca374615fb2d5a4185eccc5414
sio:SIO_000628
miriam-gene:6690
,
lld:C0149521
;
a
sio:SIO_001121
.
}
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_provenance
{
dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_assertion
dcterms:description
"[Mutations in three genes, the cationic trypsinogen (PRSS1) gene, the cystic fibrosis transmembrane conductance regulator (CFTR) gene and the pancreatic secretory trypsin inhibitor (SPINK1) gene, have been identified as risk factors for CP.]. 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:22109105
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:48+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}