@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo
> .
@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:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_head
{
this:
np:hasAssertion
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion
;
np:hasProvenance
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance
;
np:hasPublicationInfo
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion
a
np:Assertion
.
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance
a
np:Provenance
.
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion
{
miriam-gene:26580
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN08154bffac287675e7fccce76bf3fd32
sio:SIO_000628
miriam-gene:26580
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance
{
dgn-np:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion
dcterms:description
"[Further study of the pathological mechanisms of the mutant forms of seipin may lead to important new insights into motor neuron diseases, including other spastic paraplegia diseases and amyotrophic lateral sclerosis.]. 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:18790819
;
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:NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:59+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" .
}