@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0
> .
@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:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_head
{
this:
np:hasAssertion
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_assertion
;
np:hasProvenance
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_provenance
;
np:hasPublicationInfo
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_assertion
a
np:Assertion
.
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_provenance
a
np:Provenance
.
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_assertion
{
miriam-gene:181
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN68a4ba72f0b4c0f9483675a723218256
sio:SIO_000628
miriam-gene:181
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_provenance
{
dgn-np:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_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:NP392111.RADeDzxn9K6ihMefpm-7aaFl6l_3YYKw62Xm9tEYDL5h0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}