@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_head
{
this:
np:hasAssertion
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_assertion
;
np:hasProvenance
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_provenance
;
np:hasPublicationInfo
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_assertion
a
np:Assertion
.
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_provenance
a
np:Provenance
.
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0747198
a
ncit:C7057
.
dgn-gda:DGN467ae336b7064b568c992fea9c662ec9
sio:SIO_000628
miriam-gene:1080
,
lld:C0747198
;
a
sio:SIO_001121
.
}
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_provenance
{
dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_assertion
dcterms:description
"[Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with different related disorders such as congenital bilateral absence of the vas deferens, chronic idiopathic pancreatitis, or disseminated bronchiectasis (DB).]. 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:12123489
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:29+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}