@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs
> .
@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:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_head
{
this:
np:hasAssertion
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_assertion
;
np:hasProvenance
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_provenance
;
np:hasPublicationInfo
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_assertion
a
np:Assertion
.
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_provenance
a
np:Provenance
.
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_assertion
{
miriam-gene:3483
a
ncit:C16612
.
lld:C1862939
a
ncit:C7057
.
dgn-gda:DGNd45366c3da7a2313eed2b137bc487fc9
sio:SIO_000628
miriam-gene:3483
,
lld:C1862939
;
a
sio:SIO_001121
.
}
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_provenance
{
dgn-np:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_assertion
dcterms:description
"[To classify familial amyotrophic lateral sclerosis (FALS) on the base of family history, and to determine whether frequency of mutations in major amyotrophic lateral sclerosis (ALS) genes varies in different FALS categories.]. 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:22773853
;
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:NP742907.RAn9dsl1X76GgLuqDV8YFYQcXGNA3UtOMUg0hBgWumSUs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}