@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ
> .
@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:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_head
{
this:
np:hasAssertion
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_assertion
;
np:hasProvenance
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_assertion
a
np:Assertion
.
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_provenance
a
np:Provenance
.
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0398349
a
ncit:C7057
.
dgn-gda:DGNf6b2e31328db84eb50a8e328f213a825
sio:SIO_000628
miriam-gene:1080
,
lld:C0398349
;
a
sio:SIO_001121
.
}
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_provenance
{
dgn-np:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_assertion
dcterms:description
"[The aims of this study were to determine the prevalence and clinical features of distal intestinal obstruction syndrome (DIOS) and its relationship with the cystic fibrosis transmembrane conductance regulator (CFTR) genotype in an adult CF population.]. 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:15181619
;
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:NP740445.RATMmVkozsfTRQEh1l9bcj53mG2Ok7TCvMpVddRGB_DcQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}