@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_head
{
this:
np:hasAssertion
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_assertion
;
np:hasProvenance
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_provenance
;
np:hasPublicationInfo
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_assertion
a
np:Assertion
.
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_provenance
a
np:Provenance
.
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_assertion
{
miriam-gene:128674
a
ncit:C16612
.
lld:C0020619
a
ncit:C7057
.
dgn-gda:DGNb6476f3a73be5e719cd4ba19c8158fe6
sio:SIO_000628
miriam-gene:128674
,
lld:C0020619
;
a
sio:SIO_001122
.
}
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_provenance
{
dgn-np:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_assertion
dcterms:description
"[Rare variants in genes associated with idiopathic hypogonadotropic hypogonadism are found in women with hypothalamic amenorrhea, suggesting that these mutations may contribute to the variable susceptibility of women to the functional changes in GnRH secre]. 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:21247312
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP95128.RAExkPfuIFyBlUD4cJiT3U9SAY5_mxJVLDoQKxP-qWQIc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:32+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}