@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs
> .
@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:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_head
{
this:
np:hasAssertion
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_assertion
;
np:hasProvenance
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_provenance
;
np:hasPublicationInfo
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_assertion
a
np:Assertion
.
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_provenance
a
np:Provenance
.
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_assertion
{
miriam-gene:6774
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN2ef9e27206021018fb567a0d87bb1600
sio:SIO_000628
miriam-gene:6774
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_provenance
{
dgn-np:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_assertion
dcterms:description
"[We have examined oocytes from mutant C57BL/6J ob/ob mice which are both obese and infertile (although fertility can be restored by the exogenous provision of leptin) and have found STAT3 and the mutant (truncated) leptin protein to be present and polarized, suggesting the possibility that the truncated leptin protein may still contain operational domains which are functional during oocyte development and early embryogenesis.]. 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:9464852
;
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:NP817331.RAChlvb-4uZtppT3xbIh-8RVeVZRqE2abjD218VuegyLs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}