@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo
> .
@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:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_head
{
this:
np:hasAssertion
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_assertion
;
np:hasProvenance
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_provenance
;
np:hasPublicationInfo
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_assertion
a
np:Assertion
.
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_provenance
a
np:Provenance
.
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_assertion
{
miriam-gene:2896
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN6b60642de59755d1574e8a608b8d390c
sio:SIO_000628
miriam-gene:2896
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_provenance
{
dgn-np:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_assertion
dcterms:description
"[Substantial efforts have been deployed in the past decade to identify the genetic causes of amyotrophic lateral sclerosis (ALS), and we hypothesized here that mutations in SORT1 or aberrant SORT1 splicing reduce progranulin level and promote neurodegeneration.]. 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:22361451
;
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:NP557354.RAum_dQGuqDl1CNGq91Dfeesg2dUSHsOooi4P4OZQv7Uo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}