@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0
> .
@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:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_head
{
this:
np:hasAssertion
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_assertion
;
np:hasProvenance
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_provenance
;
np:hasPublicationInfo
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_assertion
a
np:Assertion
.
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_provenance
a
np:Provenance
.
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_assertion
{
miriam-gene:80199
a
ncit:C16612
.
lld:C0080174
a
ncit:C7057
.
dgn-gda:DGNcd33040e0969aa397b01eab6f8d67e13
sio:SIO_000628
miriam-gene:80199
,
lld:C0080174
;
a
sio:SIO_001121
.
}
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_provenance
{
dgn-np:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_assertion
dcterms:description
"[Spina bifida occulta, defined as a nonsymptomatic nonfusion of vertebral arches, has been suggested to be genetically determined, with an increased prevalence in patients with primary generalized epilepsy, and that the presence of this trait in fetal development can be enhanced pharmacologically to produce NTD such as meningomyelocele.]. 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:8156953
;
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:NP891656.RAKi9nSiQUSS5kbdJIpVpd-NnM6_45H8M2Fga_1f-dEr0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}