@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw
> .
@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:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_head
{
this:
np:hasAssertion
dgn-np:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_assertion
a
np:Assertion
.
dgn-np:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_provenance
a
np:Provenance
.
dgn-np:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_publicationInfo
a
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.
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dgn-np:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0028960
a
ncit:C7057
.
dgn-gda:DGN425ba3006f332764f3ec98370c8ff361
sio:SIO_000628
miriam-gene:1080
,
lld:C0028960
;
a
sio:SIO_001121
.
}
dgn-np:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_provenance
{
dgn-np:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_assertion
dcterms:description
"[To provide better insight into the relationship among the expression behavior in vivo of the three genes in human testis, analysis of MDR1 and MRP gene expression in testicular biopsies was performed and related to the presence of CFTR gene mutations in congenital absence of the vas deferens (CAVD: n = 20) and non-CAVD (n = 30) infertile patients with azoospermia or severe oligozoospermia.]. 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:11466205
;
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:NP324731.RAPRu7ppFEPpEMwJ-SVxa-MVfpWrOO3unRTZMi0JNNXOw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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
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