@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI
> .
@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:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_head
{
this:
np:hasAssertion
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_assertion
;
np:hasProvenance
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_provenance
;
np:hasPublicationInfo
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_assertion
a
np:Assertion
.
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_provenance
a
np:Provenance
.
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_assertion
{
miriam-gene:57152
a
ncit:C16612
.
lld:C2932678
a
ncit:C7057
.
dgn-gda:DGN100dc2d25d7aead9e262535eb87674fb
sio:SIO_000628
miriam-gene:57152
,
lld:C2932678
;
a
sio:SIO_001121
.
}
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_provenance
{
dgn-np:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_assertion
dcterms:description
"[Mutations in four genes encoding an ARS have been implicated in inherited peripheral neuropathy with an axonal pathology, suggesting that all ARS genes are relevant candidates for disease in patients with related phenotypes.]. 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:22930593
;
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:NP877370.RAm8w9ihNZem1Hi79vD6EnwYYINkMLG4qwu6rAdd11XDI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}