@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ
> .
@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:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_head
{
this:
np:hasAssertion
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_assertion
;
np:hasProvenance
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_assertion
a
np:Assertion
.
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_provenance
a
np:Provenance
.
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_assertion
{
miriam-gene:100653377
a
ncit:C16612
.
lld:C0041408
a
ncit:C7057
.
dgn-gda:DGN56fc9b8ec832b7e192fae2ef63dbcef6
sio:SIO_000628
miriam-gene:100653377
,
lld:C0041408
;
a
sio:SIO_001121
.
}
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_provenance
{
dgn-np:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_assertion
dcterms:description
"[DNA double-strand breaks that initiate these pathways can be alternatively resolved by crossing over between sister chromatids to form idicY chromosomes, with clinical consequences ranging from spermatogenic failure to sex reversal and Turner syndrome.]. 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:19737515
;
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:NP1016900.RAwFk6CNCcltZRKTrPiOBP7-aZYaofwcXrJOHMOP6-9BQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:48:11+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" .
}