@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM
> .
@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:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_head
{
this:
np:hasAssertion
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_assertion
;
np:hasProvenance
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_provenance
;
np:hasPublicationInfo
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_assertion
a
np:Assertion
.
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_provenance
a
np:Provenance
.
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_assertion
{
miriam-gene:27240
a
ncit:C16612
.
lld:C0037221
a
ncit:C7057
.
dgn-gda:DGN31ad0e0ac50a8a82f56dbdc3b49c9deb
sio:SIO_000628
miriam-gene:27240
,
lld:C0037221
;
a
sio:SIO_001121
.
}
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_provenance
{
dgn-np:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_assertion
dcterms:description
"[However, there are large gaps in our knowledge of the initial processes that lead to laterality defects, such as heterotaxy syndrome (HS, also known as situs ambiguous) and situs inversus totalis (SIT).]. 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:22577226
;
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:NP891542.RAYOGHbjziwNE66iUKTpknCuguixTRRJIqNw6CvMDwxWM130_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" .
}