@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ
> .
@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:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_head
{
this:
np:hasAssertion
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_assertion
;
np:hasProvenance
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_assertion
a
np:Assertion
.
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_provenance
a
np:Provenance
.
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_assertion
{
miriam-gene:8829
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN6194ec44c8b6e104436278dd6a97cb6d
sio:SIO_000628
miriam-gene:8829
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_provenance
{
dgn-np:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_assertion
dcterms:description
"[As pancreatic atrophy is rare in young adults, the patient was evaluated for cystic fibrosis by genetic testing and the patient was noted to have the deltaF508 and p.R347L mutations of the cystic fibrosis transmembrane receptor.]. 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:22787562
;
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:NP542484.RAEiae2-qziCCGLIJ-leeD89g3oMfKzt-R93dfWeB9zxQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:27+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" .
}