@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw
> .
@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:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_head
{
this:
np:hasAssertion
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_assertion
;
np:hasProvenance
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_provenance
;
np:hasPublicationInfo
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_assertion
a
np:Assertion
.
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_provenance
a
np:Provenance
.
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_assertion
{
miriam-gene:6285
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN3306f407be67360fdadb3e716d416fe7
sio:SIO_000628
miriam-gene:6285
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_provenance
{
dgn-np:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_assertion
dcterms:description
"[In humans, the gene for S100B is found on chromosome 21, within what is considered the obligate region for Down Syndrome (DS) and levels of S100B are increased in brain of both DS and Alzheimer's Disease (AD).]. 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:15126113
;
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:NP512214.RAHAUEx21g8LrHcJHAcBxKRl0CyIIieIBkqCUNYwPeGWw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}