@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco
> .
@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:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_head
{
this:
np:hasAssertion
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_assertion
;
np:hasProvenance
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_provenance
;
np:hasPublicationInfo
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_assertion
a
np:Assertion
.
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_provenance
a
np:Provenance
.
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0542519
a
ncit:C7057
.
dgn-gda:DGNb3c186509ecc370a1eafc1cb268a4ffd
sio:SIO_000628
miriam-gene:1080
,
lld:C0542519
;
a
sio:SIO_001121
.
}
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_provenance
{
dgn-np:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_assertion
dcterms:description
"[Our results showed that patients with CBAVD and renal agenesis have the same reproductive tract abnormalities as those with CUAVD, and reproductive tract abnormalities were independent of the subtypes of CFTR genotype in patients with absence of the vas deferens and CFTR gene 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:17673436
;
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:NP392034.RArWk7uvKsBjL95t92t_m4Y8u0AyqNVhOrOabe1SbDFco130_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" .
}