@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg
> .
@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:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_head
{
this:
np:hasAssertion
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_assertion
;
np:hasProvenance
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_provenance
;
np:hasPublicationInfo
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_assertion
a
np:Assertion
.
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_provenance
a
np:Provenance
.
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_assertion
{
miriam-gene:960
a
ncit:C16612
.
lld:C0028960
a
ncit:C7057
.
dgn-gda:DGNf498a6e1b07d1526a7ca54bbc99a8e07
sio:SIO_000628
miriam-gene:960
,
lld:C0028960
;
a
sio:SIO_001121
.
}
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_provenance
{
dgn-np:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_assertion
dcterms:description
"[delayed puberty), but also many unexpected findings have been made, including the lack of phenotype in women with activating LHR mutations, and the discrepancy in phenotypes of men with inactivating mutations of FSHbeta (azoospermia and infertility) and FSHR (oligozoospermia and subfertility).]. 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:16730882
;
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:NP238696.RAiYXzi6r835hez1rw4Ul13CDRGYN5BHEEDPDAm70vXZg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}