@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw
> .
@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:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_head
{
this:
np:hasAssertion
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_assertion
;
np:hasProvenance
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_assertion
a
np:Assertion
.
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_provenance
a
np:Provenance
.
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_assertion
{
miriam-gene:50511
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN401445c42482fdb220a16285c0230c45
sio:SIO_000628
miriam-gene:50511
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_provenance
{
dgn-np:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_assertion
dcterms:description
"[No functional SYCP3 exonic SNP was found in infertile Spanish patients with meiosis arrest, suggesting that SYCP3 mutations very likely are not relevant in Spain in genetic susceptibility to meiosis arrest, just as in other studied European populations.]. 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:17434513
;
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:NP708709.RASgFgQ6kOhWh7bWKzP-6Bl6rd-_HmGWHBrpxwEow0Pqw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}