@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM
> .
@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:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_head
{
this:
np:hasAssertion
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_assertion
;
np:hasProvenance
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_provenance
;
np:hasPublicationInfo
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_assertion
a
np:Assertion
.
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_provenance
a
np:Provenance
.
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_assertion
{
miriam-gene:6046
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGNf2e94a3784a8e86e1dd7c46abcfb16d2
sio:SIO_000628
miriam-gene:6046
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_provenance
{
dgn-np:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_assertion
dcterms:description
"[To verify in another population (Italians) whether a single-nucleotide polymorphism in the FSHB gene promoter previously associated with serum FSH levels in Estonians is indeed associated with sperm count and FSH plasma levels, and especially to verify whether it could be a pharmacogenetic tool for the treatment of male infertility with FSH.]. 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:22000911
;
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:NP829618.RAX5jvMRJTaW98e9w6W8WiRbLMYwehKAFMIpIQBwVJujM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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" .
}