@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64
> .
@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:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_head
{
this:
np:hasAssertion
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_assertion
;
np:hasProvenance
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_provenance
;
np:hasPublicationInfo
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_assertion
a
np:Assertion
.
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_provenance
a
np:Provenance
.
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_assertion
{
miriam-gene:1674
a
ncit:C16612
.
lld:C0878544
a
ncit:C7057
.
dgn-gda:DGN29d09458862d77a4224b65dbeda75fe3
sio:SIO_000628
miriam-gene:1674
,
lld:C0878544
;
a
sio:SIO_001122
.
}
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_provenance
{
dgn-np:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_assertion
dcterms:description
"[The lack of severe disruption of cytoskeletal desmin network formation seen with mutations in the 1A and tail domains suggests that dysfunction of seemingly intact desmin networks is sufficient to cause DCM.]. 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:17325244
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP64262.RA_3pMJ-c9cuj8MQUB1iAAxobXWj9vJ9i6CWogTNMV-64130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}