@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24
> .
@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:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_head
{
this:
np:hasAssertion
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_assertion
;
np:hasProvenance
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_provenance
;
np:hasPublicationInfo
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_assertion
a
np:Assertion
.
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_provenance
a
np:Provenance
.
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_assertion
{
miriam-gene:1282
a
ncit:C16612
.
lld:C2931784
a
ncit:C7057
.
dgn-gda:DGNc484326dd2e73bc91675276513bf573e
sio:SIO_000628
miriam-gene:1282
,
lld:C2931784
;
a
sio:SIO_001121
.
}
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_provenance
{
dgn-np:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_assertion
dcterms:description
"[Two forms of inherited intracerebral hemorrhage (ICH) are associated with an amyloid angiopathy caused by mutations in the genes for the amyloid precursor protein or cystatin C. The purpose of this study was to determine whether patients with sporadic ICH have mutations in the amyloid precursor protein or cystatin C genes.]. 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:7945009
;
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:NP796957.RAaTEiEFvkkIWn6E99q0DqRAJiwV7gfMGDIsNTPf8NT24130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}