@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8
> .
@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:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_head
{
this:
np:hasAssertion
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_assertion
;
np:hasProvenance
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_provenance
;
np:hasPublicationInfo
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_assertion
a
np:Assertion
.
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_provenance
a
np:Provenance
.
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0566602
a
ncit:C7057
.
dgn-gda:DGN82c84f338f35864e0d3a12c6a8d3f6f8
sio:SIO_000628
miriam-gene:1080
,
lld:C0566602
;
a
sio:SIO_001121
.
}
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_provenance
{
dgn-np:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_assertion
dcterms:description
"[Because biliary tract lesions that resemble those of primary sclerosing cholangitis (PSC) may occur in cystic fibrosis (CF), we examined the prevalence and influence of CF transmembrane conductance regulator (CFTR) gene mutations in PSC patients.]. 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:12127423
;
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:NP529883.RAeoW76sByXIX6CCUPEPqjtlZX8ULf6FfHFxMoyBTiEj8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:20+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" .
}