@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI
> .
@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:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_head
{
this:
np:hasAssertion
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_assertion
;
np:hasProvenance
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_provenance
;
np:hasPublicationInfo
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_assertion
a
np:Assertion
.
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_provenance
a
np:Provenance
.
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_assertion
{
miriam-gene:2332
a
ncit:C16612
.
lld:C0242354
a
ncit:C7057
.
dgn-gda:DGN1231d00b8ed5f3a66700d544056e67a0
sio:SIO_000628
miriam-gene:2332
,
lld:C0242354
;
a
sio:SIO_001121
.
}
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_provenance
{
dgn-np:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_assertion
dcterms:description
"[In dealing with patients who are found to have fragile sites, other than FRAXA, FRAXE and possibly FRA11B, considerable reassurance can be given that they are not at increased risk of having children with congenital disease or developing disease themselves because of their fragile sites.]. 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:11076037
;
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:NP798790.RAC5gHw_-7XuC5473_uRP1FF0n7f_OyaLXABgwX34jscI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}