@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY
> .
@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:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_head
{
this:
np:hasAssertion
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_assertion
;
np:hasProvenance
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_provenance
;
np:hasPublicationInfo
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_assertion
a
np:Assertion
.
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_provenance
a
np:Provenance
.
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_assertion
{
miriam-gene:867
a
ncit:C16612
.
lld:C0242354
a
ncit:C7057
.
dgn-gda:DGNc0d5d1e2776efb047f8414f98d30a9c7
sio:SIO_000628
miriam-gene:867
,
lld:C0242354
;
a
sio:SIO_001121
.
}
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_provenance
{
dgn-np:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_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:NP344904.RAMMGRPmYb_Rplp8p8WhveB5Vfwb9E40Kma5Yj_aeqGdY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}