@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA
> .
@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:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_head
{
this:
np:hasAssertion
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_assertion
;
np:hasProvenance
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_provenance
;
np:hasPublicationInfo
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_assertion
a
np:Assertion
.
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_provenance
a
np:Provenance
.
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGNd5d8ae9c0bb612078a0f4746784e9eb6
sio:SIO_000628
miriam-gene:351
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_provenance
{
dgn-np:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_assertion
dcterms:description
"[The amyloid deposition in familial forms of inclusion body myopathy may be either due to errors in other gene loci, or it is secondary reflecting altered beta APP metabolism or myocyte degeneration and cell membrane degradation.]. 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:7654077
;
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:NP758709.RATslb4Q_kUVgl_QUia7PtWYae5BK1xR4xh0IGkDrJeeA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:39+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" .
}