@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk
> .
@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:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_head
{
this:
np:hasAssertion
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_assertion
;
np:hasProvenance
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_provenance
;
np:hasPublicationInfo
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_assertion
a
np:Assertion
.
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_provenance
a
np:Provenance
.
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_assertion
{
miriam-gene:410
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN41957899ffb877bd70dbf42bbb878005
sio:SIO_000628
miriam-gene:410
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_provenance
{
dgn-np:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_assertion
dcterms:description
"[Here, we report a novel method for the sensitive detection of misfolded huntingtin (HTT) isolated from the brains of transgenic (Tg) mouse models of HD and humans with HD using an amyloid seeding assay (ASA), which is based on the propensity of misfolded proteins to act as a seed and shorten the nucleation-associated lag phase in the kinetics of amyloid formation in vitro.]. 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:22187438
;
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:NP380258.RAhRUScjM8UZWPabeSr8uwu__R27rqucOMdZj66-Wb7Sk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:45+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" .
}