@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU
> .
@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:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_head
{
this:
np:hasAssertion
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_assertion
;
np:hasProvenance
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_provenance
;
np:hasPublicationInfo
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_assertion
a
np:Assertion
.
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_provenance
a
np:Provenance
.
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_assertion
{
miriam-gene:9541
a
ncit:C16612
.
lld:C0016412
a
ncit:C7057
.
dgn-gda:DGNe6b6af7d36b3a31c528d4e95d0c628b1
sio:SIO_000628
miriam-gene:9541
,
lld:C0016412
;
a
sio:SIO_001121
.
}
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_provenance
{
dgn-np:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_assertion
dcterms:description
"[It was concluded that the FUS, CIR, and HS morphologies represent promising biomarkers of CIN that are sensitive to folate deficiency, and further validation and investigation of the mechanisms responsible for their formation is warranted.]. 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:22430981
;
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:NP227006.RAmjXBn_xpqycq3qX7rjdbeJtbmDdHtSGtNdLhFWf56tU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:06+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" .
}