@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w
> .
@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:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_head
{
this:
np:hasAssertion
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_assertion
;
np:hasProvenance
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_provenance
;
np:hasPublicationInfo
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_assertion
a
np:Assertion
.
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_provenance
a
np:Provenance
.
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0751587
a
ncit:C7057
.
dgn-gda:DGNd10258ff9552e92244003d65b1205f84
sio:SIO_000628
miriam-gene:4854
,
lld:C0751587
;
a
sio:SIO_001121
.
}
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_provenance
{
dgn-np:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_assertion
dcterms:description
"[Linked to autosomal dominant mutations in diverse genes that encode cell-surface receptors (i.e., amyloid precursor protein in CAA and NOTCH3 in CADASIL), both diseases are associated with accumulation of abnormal material around cerebral vessels, such as amyloid in CAA or granular osmiophilic material in CADASIL.]. 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:22137428
;
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:NP943607.RA1RmCYR3Ts1npxPdvNFRPvVR_DmAVDEU0V0jnYXYd53w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:52+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" .
}