@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY
> .
@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:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_head
{
this:
np:hasAssertion
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_assertion
;
np:hasProvenance
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_provenance
;
np:hasPublicationInfo
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_assertion
a
np:Assertion
.
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_provenance
a
np:Provenance
.
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0025286
a
ncit:C7057
.
dgn-gda:DGNfeb03765ad6cd42ef4801ee3efd86f84
sio:SIO_000628
miriam-gene:3077
,
lld:C0025286
;
a
sio:SIO_001121
.
}
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_provenance
{
dgn-np:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_assertion
dcterms:description
"[Notable findings include high expression of transferrin receptor 1 in the hippocampus and medulla oblongata compared to other brain regions, low expression of HFE in normal brain with elevated HFE expression in meningiomas, and absence of hepcidin mRNA in astrocytoma cell lines despite expression in normal brain and tumor specimens.]. 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:19386095
;
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:NP763139.RAF3dNny73a7xbvSr8vcnOLTaMHneV9xP11a9vhJDcLuY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}