@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU
> .
@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:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_head
{
this:
np:hasAssertion
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_assertion
;
np:hasProvenance
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_provenance
;
np:hasPublicationInfo
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_assertion
a
np:Assertion
.
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_provenance
a
np:Provenance
.
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_assertion
{
miriam-gene:6690
a
ncit:C16612
.
lld:C0030305
a
ncit:C7057
.
dgn-gda:DGN16d8aef52030db7c6adead8505950de9
sio:SIO_000628
miriam-gene:6690
,
lld:C0030305
;
a
sio:SIO_001121
.
}
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_provenance
{
dgn-np:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_assertion
dcterms:description
"[The role of mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) as well as the pancreatic secretory trypsin inhibitor (PSTI) in patients with pancreatitis is intriguing but as yet incompletely understood.]. 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:11276378
;
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:NP263117.RAeDBrUV0N5u3stnBin4FjiA5kPdJEsyRHD62nqJK5PfU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}