@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs
> .
@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:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_head
{
this:
np:hasAssertion
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_assertion
;
np:hasProvenance
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_provenance
;
np:hasPublicationInfo
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_assertion
a
np:Assertion
.
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_provenance
a
np:Provenance
.
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_assertion
{
miriam-gene:5663
a
ncit:C16612
.
lld:C0003635
a
ncit:C7057
.
dgn-gda:DGN9b80e9120bf6caec396144901761873c
sio:SIO_000628
miriam-gene:5663
,
lld:C0003635
;
a
sio:SIO_001121
.
}
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_provenance
{
dgn-np:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_assertion
dcterms:description
"[Clinical manifestation of these patients included memory loss, counting difficulty, personality change, disorientation, dyscalculia, agnosia, aphasia, and apraxia, which was similar to that of the familial AD (FAD) patients harboring other PS1 mutations.]. 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:24737487
;
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:NP1173968.RAiTbFT8x-mY0Ca4Dt4XhWHkaN_0ME13OrdJMhieXb8Cs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:38+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" .
}