@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo
> .
@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:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_head
{
this:
np:hasAssertion
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_assertion
;
np:hasProvenance
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_provenance
;
np:hasPublicationInfo
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_assertion
a
np:Assertion
.
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_provenance
a
np:Provenance
.
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0403814
a
ncit:C7057
.
dgn-gda:DGN9c3865bcfd646672b89f297a45a66517
sio:SIO_000628
miriam-gene:1080
,
lld:C0403814
;
a
sio:SIO_001121
.
}
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_provenance
{
dgn-np:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_assertion
dcterms:description
"[To investigate whether genetic modifiers of cystic fibrosis (CF) lung disease also predispose to congenital bilateral absence of the vas deferens (CBAVD) in association with cystic fibrosis transmembrane conductance regulator (CFTR) mutations.]. 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:20100616
;
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:NP789284.RAw3yJ5j5esdtwuYg-McYs46qMinw1n7O42mTjxLROsRo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:43+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" .
}