@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8
> .
@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:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_assertion
a
np:Assertion
.
dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_provenance
a
np:Provenance
.
dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_assertion
{
miriam-gene:5428
a
ncit:C16612
.
lld:C0025322
a
ncit:C7057
.
dgn-gda:DGN7266fd920e4af6701b9858000df6ad8f
sio:SIO_000628
miriam-gene:5428
,
lld:C0025322
;
a
sio:SIO_001121
.
}
dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_provenance
{
dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_assertion
dcterms:description
"[The study objective was to determine if mutations in mitochondrial DNA polymerase gamma (POLG) are associated with spontaneous 46,XX primary ovarian insufficiency (sPOI) using restriction fragment length polymorphism analysis of genomic DNA.]. 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:20701905
;
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 .
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dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}