@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY
> .
@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:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_head
{
this:
np:hasAssertion
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_assertion
;
np:hasProvenance
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_provenance
;
np:hasPublicationInfo
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_assertion
a
np:Assertion
.
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_provenance
a
np:Provenance
.
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_assertion
{
miriam-gene:6311
a
ncit:C16612
.
lld:C1862939
a
ncit:C7057
.
dgn-gda:DGNfccca0db7056b201cd415e4fbd3c72e2
sio:SIO_000628
miriam-gene:6311
,
lld:C1862939
;
a
sio:SIO_001121
.
}
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_provenance
{
dgn-np:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_assertion
dcterms:description
"[Screening for SOD1, TARDBP, FUS, ANG, ATXN2, OPTN, and C9ORF72 was carried out in 480 consecutive patients with sporadic ALS (SALS) and in 48 familial ALS (FALS) index patients admitted to a single Italian referral center.]. 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:22722621
;
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:NP660965.RAR3U7RmTFm90wfRkt5Y0NSBHnT6GJIdqso8HbfwS4uZY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}