@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_head
{
this:
np:hasAssertion
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_assertion
;
np:hasProvenance
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_provenance
;
np:hasPublicationInfo
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_assertion
a
np:Assertion
.
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_provenance
a
np:Provenance
.
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_assertion
{
miriam-gene:4803
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN13cddc79050faa8b873b374d9d2bf7f3
sio:SIO_000628
miriam-gene:4803
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_provenance
{
dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_assertion
dcterms:description
"[Most Tg AD models, which at least partly recapitulate the AD phenotype, are based on insertion of one or more human mutations (identified in Familial AD) into the mouse genome, with the notable exception of the anti-NGF mouse, which is based on the cholinergic unbalance hypothesis.]. 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:21732714
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:35+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}