@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc
> .
@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:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_head
{
this:
np:hasAssertion
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_assertion
;
np:hasProvenance
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_provenance
;
np:hasPublicationInfo
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_assertion
a
np:Assertion
.
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_provenance
a
np:Provenance
.
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_assertion
{
miriam-gene:7031
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGNfe771e1a873a3f7ac9cbf2233b546a3b
sio:SIO_000628
miriam-gene:7031
,
lld:C0162534
;
a
sio:SIO_001121
.
}
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_provenance
{
dgn-np:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_assertion
dcterms:description
"[Mutations in the genes encoding the presenilins (PS1 and PS2) and amyloid precursor protein (APP) are associated with FAD, whereas mutations in the prion protein (PrP) gene are associated with prion disease.]. 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:10631141
;
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:NP199765.RAmnl8Zj-9zZ_LfdO3HaWphSpkuY0yZHmozJi5JjRubhc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}