@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM
> .
@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:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_head
{
this:
np:hasAssertion
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_assertion
;
np:hasProvenance
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_provenance
;
np:hasPublicationInfo
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_assertion
a
np:Assertion
.
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_provenance
a
np:Provenance
.
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0028960
a
ncit:C7057
.
dgn-gda:DGN4803d4a7b8007527975490bf140bbca2
sio:SIO_000628
miriam-gene:4524
,
lld:C0028960
;
a
sio:SIO_001121
.
}
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_provenance
{
dgn-np:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_assertion
dcterms:description
"[The objective of this study was to analyze the distribution of the methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms in idiopathic infertile Brazilian patients with nonobstructive azoospermia (NOA) or severe oligozoospermia and fertile Brazilian men as controls to explore the possible association of these polymorphisms and male infertility.]. 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:21138341
;
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:NP224384.RAkfRloQU2H_hXTKkT82A7d1Lxub9VNsV7IX39s_eciwM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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
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}