@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY
> .
@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:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_head
{
this:
np:hasAssertion
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_assertion
;
np:hasProvenance
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_provenance
;
np:hasPublicationInfo
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_assertion
a
np:Assertion
.
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_provenance
a
np:Provenance
.
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_assertion
{
miriam-gene:4548
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGN9040a7af92d9c90f37e43c518075fb50
sio:SIO_000628
miriam-gene:4548
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_provenance
{
dgn-np:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_assertion
dcterms:description
"[None of the polymorphisms were significantly associated with idiopathic male infertility after the implementation of Bonferroni correction for multiple testing, although the MTHFD1 G1958A and MTR A2756G polymorphisms showed an association before the Bonferroni correction.]. 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:24268703
;
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:NP735273.RAc83CWR3NzjR3bfqOPtsZpVtsZilfOgOhRumeHGMc0bY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:26+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" .
}