@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4
> .
@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:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_head
{
this:
np:hasAssertion
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_assertion
;
np:hasProvenance
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_provenance
;
np:hasPublicationInfo
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_assertion
a
np:Assertion
.
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_provenance
a
np:Provenance
.
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_assertion
{
miriam-gene:2796
a
ncit:C16612
.
lld:C0271623
a
ncit:C7057
.
dgn-gda:DGN46338470175517ea0b51d0925597daa9
sio:SIO_000628
miriam-gene:2796
,
lld:C0271623
;
a
sio:SIO_001121
.
}
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_provenance
{
dgn-np:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_assertion
dcterms:description
"[The discovery in 1977 of a hypogonadal mouse lacking GnRH (hpg mice) and, in 1986, that the gnrh1 gene was deleted in this mouse, suggested that GNRH1 mutations might also cause human congenital idiopathic (or isolated) hypogonadotropic hypogonadism.]. 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:20389089
;
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:NP335269.RAzuU1Rt5Vqy7eFHGQbLTCiADkIZKWfK_P8YQuMvzowv4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}