@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY
> .
@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:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_head
{
this:
np:hasAssertion
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_assertion
;
np:hasProvenance
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_assertion
a
np:Assertion
.
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_provenance
a
np:Provenance
.
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C1862939
a
ncit:C7057
.
dgn-gda:DGN0ff6c07da520a64bfa4ef50ea2102b44
sio:SIO_000628
miriam-gene:6647
,
lld:C1862939
;
a
sio:SIO_001121
.
}
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_provenance
{
dgn-np:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_assertion
dcterms:description
"[The discovery of mutations in the human SOD1 gene encoding Cu,Zn superoxide dismutase (Cu,Zn SOD) in patients with familial amyotrophic lateral sclerosis (ALS) has made possible the development of etiological models of the disease.]. 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:9419057
;
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:NP1386368.RALekYkqjCNBqku2u7EdIyMUUVRv3KwHXVdZrKA1KyYnY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:14+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" .
}