@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE
> .
@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:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_head
{
this:
np:hasAssertion
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_assertion
;
np:hasProvenance
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_provenance
;
np:hasPublicationInfo
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_assertion
a
np:Assertion
.
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_provenance
a
np:Provenance
.
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_assertion
{
miriam-gene:23064
a
ncit:C16612
.
lld:C0587246
a
ncit:C7057
.
dgn-gda:DGN6ac009a352b89419ce347bf510dfbb15
sio:SIO_000628
miriam-gene:23064
,
lld:C0587246
;
a
sio:SIO_001121
.
}
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_provenance
{
dgn-np:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_assertion
dcterms:description
"[ALS4 is a juvenile-onset, autosomal dominant form of ALS that is characterized by slow progression, distal limb weakness and amyotrophy, and pyramidal signs associated with severe loss of motor neurons in the brain and spinal cord.]. 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:11085590
;
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:NP470703.RAQo1SJ6fbBURSpVqR9r23v3IQX8CEVtGwcLDnBDvrLdE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}