@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA
> .
@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:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_head
{
this:
np:hasAssertion
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_assertion
;
np:hasProvenance
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_provenance
;
np:hasPublicationInfo
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_assertion
a
np:Assertion
.
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_provenance
a
np:Provenance
.
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGNd9dc4e012ba47d71a0ccdae4d2b92cea
sio:SIO_000628
miriam-gene:3077
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_provenance
{
dgn-np:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_assertion
dcterms:description
"[The aim of this study was to find out whether C282Y and H63D mutations in the hemochromatosis (HFE) gene are associated with male infertility and whether the prevalence of the HFE mutations is higher in a group of 262 infertile men in comparison to 200 fertile men.]. 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:17067586
;
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:NP375215.RAh36kv80te0n9coIbXYxGawJjLqMCexMoEqYC5zHZjhA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}