@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls
> .
@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:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_head
{
this:
np:hasAssertion
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_assertion
;
np:hasProvenance
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_provenance
;
np:hasPublicationInfo
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_assertion
a
np:Assertion
.
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_provenance
a
np:Provenance
.
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN9d1c23ce1fa24f856dd860b72eee30f3
sio:SIO_000628
miriam-gene:3077
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_provenance
{
dgn-np:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_assertion
dcterms:description
"[The aim of this study was to screen infertile men for HFE H63D mutation in correlation with clinical characteristics of infertile men (sperm concentration, sperm motility, morphology, testicular volume, Follicle Stimulating Hormone (FSH), Luteinizing Hormone (LH) and total Testosterone levels) and find out if the HFE H63D mutation has an effect on 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:18846434
;
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:NP466345.RAhdG05ovKvxUAJLG7r_QXJMpQyzmS-KV5rYKzJ1shqls130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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" .
}