@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg
> .
@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:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_head
{
this:
np:hasAssertion
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_assertion
;
np:hasProvenance
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_provenance
;
np:hasPublicationInfo
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_assertion
a
np:Assertion
.
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_provenance
a
np:Provenance
.
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_assertion
{
miriam-gene:2539
a
ncit:C16612
.
lld:C0008533
a
ncit:C7057
.
dgn-gda:DGNd85f62525eb385e2f92449237658b52d
sio:SIO_000628
miriam-gene:2539
,
lld:C0008533
;
a
sio:SIO_001121
.
}
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_provenance
{
dgn-np:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_assertion
dcterms:description
"[The findings described herein and the knowledge that Factor IX deficiency recombines freely with at least two loci of the G6PD cluster support our hypothesis that the chromosomal region which includes the fragile-X site is normally a region of high meiotic recombination.]. 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:3924593
;
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:NP731812.RA53qMKbGe3_1pV1QD7HcWABppPfCCs9zpfWl25rqbmIg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+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" .
}