@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw
> .
@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:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_head
{
this:
np:hasAssertion
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_assertion
;
np:hasProvenance
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_provenance
;
np:hasPublicationInfo
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_assertion
a
np:Assertion
.
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_provenance
a
np:Provenance
.
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_assertion
{
miriam-gene:4487
a
ncit:C16612
.
lld:C0020608
a
ncit:C7057
.
dgn-gda:DGNa7c23587d78db13fd0de68753b412192
sio:SIO_000628
miriam-gene:4487
,
lld:C0020608
;
a
sio:SIO_001121
.
}
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_provenance
{
dgn-np:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_assertion
dcterms:description
"[In the three sisters reported, their common oligodontia phenotype is not caused by mutations in the coding regions of MSX1, PAX9, AXIN2, DLX1 or DLX2 genes, but genetic factors most probably play a role as all three sisters were affected.]. 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:18199077
;
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:NP303619.RAKPCPHogM92b9bYptp0rQ86kOdw0f2I9G3jWzSw2OVCw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:54+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" .
}