@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k
> .
@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:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_head
{
this:
np:hasAssertion
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_assertion
;
np:hasProvenance
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_provenance
;
np:hasPublicationInfo
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_assertion
a
np:Assertion
.
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_provenance
a
np:Provenance
.
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN7e09aeffd2d3732f83e01c2d64a053c8
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_provenance
{
dgn-np:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_assertion
dcterms:description
"[Mutations in the cystic fibrosis (CF) conductance transmembrane regulator (CFTR) gene have been detected in patients with CF and in males with infertility attributable to congenital bilateral absence of the 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:7532150
;
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:NP1310991.RAy7hIlc5SESNto57JPyWJy2XJLa6GGeuzsY7rpkTwQ2k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:40+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" .
}