@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA
> .
@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/v3.0.0/void/
> .
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_head
{
this:
np:hasAssertion
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_assertion
;
np:hasProvenance
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_provenance
;
np:hasPublicationInfo
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_assertion
a
np:Assertion
.
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_provenance
a
np:Provenance
.
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_assertion
{
miriam-gene:7534
a
ncit:C16612
.
lld:C0270724
a
ncit:C7057
.
dgn-gda:DGN8e73b904ad9a422377bd3d0b8d1f34ad
sio:SIO_000628
miriam-gene:7534
,
lld:C0270724
;
a
sio:SIO_001121
.
}
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_provenance
{
dgn-np:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_assertion
dcterms:description
"[The disorder demonstrated a type and distribution of lesions homologous to that of human infantile neuroaxonal dystrophy (INAD), most commonly caused by mutations of phospholipase A2 group VI gene (PLA2G6), but alleles of informative markers flanking the canine PLA2G6 locus did not associate with the canine disorder.]. 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:20653033
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP781835.RASOyF08VlxqtBS69EwqdiNdXGcdpngPGBOO8oEPD6-KA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:32+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}