@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y
> .
@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:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_head
{
this:
np:hasAssertion
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_assertion
;
np:hasProvenance
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_assertion
a
np:Assertion
.
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_provenance
a
np:Provenance
.
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_assertion
{
miriam-gene:10625
a
ncit:C16612
.
lld:C0917796
a
ncit:C7057
.
dgn-gda:DGN7a2315aae589f06986482cda2a7591d2
sio:SIO_000628
miriam-gene:10625
,
lld:C0917796
;
a
sio:SIO_001121
.
}
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_provenance
{
dgn-np:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_assertion
dcterms:description
"[Biochemical and molecular genetic evidence is presented that in six independent pedigrees the development of Leber hereditary optic neuropathy (LHON) is due to the same primary mutation in the mitochondrial ND1 gene.]. 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:1928099
;
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:NP220448.RASiTG_A-QevtNyOrEuME0ZBn0ZE7fDBN1hSkpy8xFX1Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}