@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_assertion
;
np:hasProvenance
dgn-np:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_provenance
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np:hasPublicationInfo
dgn-np:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_assertion
a
np:Assertion
.
dgn-np:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_provenance
a
np:Provenance
.
dgn-np:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2100
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN3521ef9c50b63438875a24961f544048
sio:SIO_000628
miriam-gene:2100
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_provenance
{
dgn-np:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_assertion
dcterms:description
"[To examine whether polymorphisms within the ESR1, FSHR, ESR2, CYP19A1, and NRIP1 genes are susceptibility factors for human male idiopathic infertility and to test the joint effects of these genes on male reproductive function.]. 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:16213843
;
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:NP255644.RARc4-3BPNWBasrhU3JAcqYZo_gMdYcqQXg2c7Eo9psps130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
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"v2.1.0" .
}