@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA
> .
@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:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_head
{
this:
np:hasAssertion
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_assertion
;
np:hasProvenance
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_provenance
;
np:hasPublicationInfo
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_assertion
a
np:Assertion
.
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_provenance
a
np:Provenance
.
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNc9afe5d470c5648f5ca0e96eefd1e62a
sio:SIO_000628
miriam-gene:6647
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_provenance
{
dgn-np:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_assertion
dcterms:description
"[However, because only a subset of cases can be attributed to one particular molecular defect (such as mutation of SOD1 or the gene encoding neurofilament H), the aetiology of ALS is likely to be multifactorial.]. 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:11724913
;
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:NP337593.RA-Gh1Sxr0yue8sVqj9w7FlKUx9Yk-ieQMeLluoRIyEnA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:18+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" .
}