@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw
> .
@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:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_head
{
this:
np:hasAssertion
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_assertion
;
np:hasProvenance
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_provenance
;
np:hasPublicationInfo
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_assertion
a
np:Assertion
.
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_provenance
a
np:Provenance
.
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_assertion
{
miriam-gene:8313
a
ncit:C16612
.
lld:C0020608
a
ncit:C7057
.
dgn-gda:DGN0a2b6dd719cd10623ec28a0cd6b1172c
sio:SIO_000628
miriam-gene:8313
,
lld:C0020608
;
a
sio:SIO_001121
.
}
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_provenance
{
dgn-np:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_assertion
dcterms:description
"[Considering the discrepancy between the high incidence rate of agenesis and the relatively small number of reported causative mutations in PAX9, MSX1 and AXIN2 genes, the genetic contribution to oligodontia probably is much more heterogeneous than expected so far.]. 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:16918677
;
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:NP689191.RAzTx57_6ZgkueBi3DHuxIA3kEE68V_0E1sVKyv4WQqQw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}