@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8
> .
@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:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_head
{
this:
np:hasAssertion
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_assertion
;
np:hasProvenance
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_provenance
;
np:hasPublicationInfo
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_assertion
a
np:Assertion
.
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_provenance
a
np:Provenance
.
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_assertion
{
miriam-gene:6550
a
ncit:C16612
.
lld:C0037859
a
ncit:C7057
.
dgn-gda:DGN241f3578f11e7994d22c7d0c199010f1
sio:SIO_000628
miriam-gene:6550
,
lld:C0037859
;
a
sio:SIO_001121
.
}
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_provenance
{
dgn-np:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_assertion
dcterms:description
"[Tissue-specific co-expression with CFTR and NHE3 supports diverse functions of SLC26A3 and may have an impact on pathophysiology of male subfertility both in CLD and in cystic fibrosis (CF), as well as spermatoceles.]. 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:16421216
;
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:NP768281.RAHz0qS-VsHDy8jFP1CeMQW8pY6-QQClTbEOvgHS8f3P8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}