@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o
> .
@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:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_head
{
this:
np:hasAssertion
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_assertion
;
np:hasProvenance
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_provenance
;
np:hasPublicationInfo
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_assertion
a
np:Assertion
.
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_provenance
a
np:Provenance
.
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0747198
a
ncit:C7057
.
dgn-gda:DGN3d8adaf89bc371a2e71aeeadf58fe6e1
sio:SIO_000628
miriam-gene:1080
,
lld:C0747198
;
a
sio:SIO_001121
.
}
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_provenance
{
dgn-np:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_assertion
dcterms:description
"[Patients with cystic fibrosis and unexplained upper abdominal pain should be screened for pancreatitis, and consideration should be given to screening patients with idiopathic pancreatitis for mutations in the CFTR gene.]. 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:12422349
;
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:NP217026.RAKaB2_rEgwF2URSTDJM0hKtwewxq_UruYijvOdahVv3o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}