@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU
> .
@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:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_head
{
this:
np:hasAssertion
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_assertion
;
np:hasProvenance
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_provenance
;
np:hasPublicationInfo
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_assertion
a
np:Assertion
.
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_provenance
a
np:Provenance
.
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_assertion
{
miriam-gene:181
a
ncit:C16612
.
lld:C0332910
a
ncit:C7057
.
dgn-gda:DGNfcd3ee3bc498a93268954b2ee98842bd
sio:SIO_000628
miriam-gene:181
,
lld:C0332910
;
a
sio:SIO_001121
.
}
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_provenance
{
dgn-np:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_assertion
dcterms:description
"[Genetic testing of the cystic fibrosis transmembrane conductance (CFTR) gene is currently performed in couples undergoing assisted reproduction techniques (ART), because of the high prevalence of healthy carriers in the population and the pathogenic relationship with congenital bilateral absence of vas deferens (CBAVD).]. 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:15870824
;
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:NP595317.RAERU-4TRhgq9FHhU5I5me1H0TU05wzEEHUT0FbPEtJMU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:58+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" .
}