@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_assertion
;
np:hasProvenance
dgn-np:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_provenance
;
np:hasPublicationInfo
dgn-np:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_assertion
a
np:Assertion
.
dgn-np:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_provenance
a
np:Provenance
.
dgn-np:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:367
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN1df9224049b7b6726f0592d775703933
sio:SIO_000628
miriam-gene:367
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_provenance
{
dgn-np:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_assertion
dcterms:description
"[We have analysed this CAG repeat sequence in a large number of patients with typical sporadic ALS and in normal controls, in order to test the hypothesis that this polymorphism of the androgen receptor gene may influence susceptibility for ALS.]. 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:8400860
;
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:NP639009.RAJoeyTyR4rYFnCAbMznE8U_RZrrqy8tftICBaxsA_Lwc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:25+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
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pav:authoredBy
<
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> , <
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> , <
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
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"v2.1.0" .
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