@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s
> .
@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:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_head
{
this:
np:hasAssertion
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_assertion
;
np:hasProvenance
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_provenance
;
np:hasPublicationInfo
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_assertion
a
np:Assertion
.
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_provenance
a
np:Provenance
.
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_assertion
{
miriam-gene:4513
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGNa27ec46c6c3d861347e73348ddceb43d
sio:SIO_000628
miriam-gene:4513
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_provenance
{
dgn-np:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_assertion
dcterms:description
"[Recently, a significantly higher ratio of nucleotide changes in the mtDNA genes: COII, ATPase 6, ATPase 8, ND2, ND3, ND4, and ND5 was reported in spermatozoa from populations of infertile Indian men, compared suggesting that screening for mtDNA mutations could provide insight into the aetiology of male infertility.]. 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:22089605
;
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:NP747514.RA3ewQU8BGY2e5nuWMVOoDNlXdpEPG5ojsrNLoMbAUZ7s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}