@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA
> .
@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:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_head
{
this:
np:hasAssertion
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_assertion
;
np:hasProvenance
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_provenance
;
np:hasPublicationInfo
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_assertion
a
np:Assertion
.
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_provenance
a
np:Provenance
.
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_assertion
{
miriam-gene:2492
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGN95ee2dbea43b139ef9d3d3ae408ffd7f
sio:SIO_000628
miriam-gene:2492
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_provenance
{
dgn-np:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_assertion
dcterms:description
"[Our findings suggest that the FSHR polymorphisms at the studied sites do not associate with idiopathic male infertility and have no influence on FSH levels both in normal and infertile males in the Han-Chinese population.]. 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:21334319
;
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:NP547563.RAqGmp0T-2TmkuPot2wg9WOK6i5B79F09p1V4W8sH8AGA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:30+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" .
}