@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc
> .
@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:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_head
{
this:
np:hasAssertion
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_assertion
;
np:hasProvenance
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_provenance
;
np:hasPublicationInfo
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_assertion
a
np:Assertion
.
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_provenance
a
np:Provenance
.
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNb064977128778177db529d2890428efe
sio:SIO_000628
miriam-gene:2837
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_provenance
{
dgn-np:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_assertion
dcterms:description
"[The second is the pathological aspect: iron chelating compounds target the APP 5'UTR and possess the capacity to reduce APP translation, and subsequently Abeta levels, and thus represent molecules with high potential in the development of drugs for the treatment of 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:19090990
;
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:NP215870.RALJWoKkOnRlny7ONbN6oLhwb3jnwIRVn4Fm6YPo2EuOc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}