@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50
> .
@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:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_head
{
this:
np:hasAssertion
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_assertion
;
np:hasProvenance
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_provenance
;
np:hasPublicationInfo
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_assertion
a
np:Assertion
.
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_provenance
a
np:Provenance
.
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_assertion
{
miriam-gene:5644
a
ncit:C16612
.
lld:C0030297
a
ncit:C7057
.
dgn-gda:DGNa8d78d5f350dc9476ae5b5583b194a19
sio:SIO_000628
miriam-gene:5644
,
lld:C0030297
;
a
sio:SIO_001122
.
}
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_provenance
{
dgn-np:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_assertion
dcterms:description
"[The genotype of the Danish population with HP differs from that of previously described cohorts. The occurrence of exocrine and endocrine insufficiency is higher among patients with HP than in patients with SPINK1-CFTR mutations and tIP, and more HP famil]. 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:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP87947.RAPfryuJCoUeDTRrE8J6Una_8NhGWYgQDEzDM5Xi-CJ50130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:28+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: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" .
}