@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs
> .
@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:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_head
{
this:
np:hasAssertion
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_assertion
;
np:hasProvenance
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_provenance
;
np:hasPublicationInfo
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_assertion
a
np:Assertion
.
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_provenance
a
np:Provenance
.
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_assertion
{
miriam-gene:4015
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNd15214cb75712cb6cf2089974d4f084c
sio:SIO_000628
miriam-gene:4015
,
lld:C0002736
;
a
sio:SIO_001122
.
}
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_provenance
{
dgn-np:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_assertion
dcterms:description
"[Polymorphisms of the LOX gene were genotyped in 192 ALS patients, including 31 unrelated familial cases and 138 controls, and no association was found between any of these polymorphisms and amyotrophic lateral sclerosis or its phenotype.]. 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:11675877
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP140654.RA80PHY4PYPAjI1Sb0lbGpVDJHlGn41j1BaZ85ktxrHCs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:13+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" .
}