@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg
> .
@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:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_head
{
this:
np:hasAssertion
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_assertion
;
np:hasProvenance
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_provenance
;
np:hasPublicationInfo
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_assertion
a
np:Assertion
.
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_provenance
a
np:Provenance
.
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_assertion
{
miriam-gene:23552
a
ncit:C16612
.
lld:C0233794
a
ncit:C7057
.
dgn-gda:DGN881bce62736e5989e7d6620e94414cf6
sio:SIO_000628
miriam-gene:23552
,
lld:C0233794
;
a
sio:SIO_001121
.
}
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_provenance
{
dgn-np:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_assertion
dcterms:description
"[However, mice that remained hippocampally iron deficient until P42 continued to have spatial memory deficits, impaired CA1 apical dendrite structure, and persistent alterations in PV and PNN expression and reduced BDNF despite iron repletion.]. 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:22367974
;
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:NP910662.RAHNIXCfqFMOo2ovSCXZH1K1Bk-KqKNXfm03MZSNBS_Hg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}