@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI
> .
@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:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_head
{
this:
np:hasAssertion
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_assertion
;
np:hasProvenance
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_provenance
;
np:hasPublicationInfo
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_assertion
a
np:Assertion
.
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_provenance
a
np:Provenance
.
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_assertion
{
miriam-gene:5083
a
ncit:C16612
.
lld:C0399352
a
ncit:C7057
.
dgn-gda:DGNc67736601cad199cd943b3a0c8ea938f
sio:SIO_000628
miriam-gene:5083
,
lld:C0399352
;
a
sio:SIO_001121
.
}
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_provenance
{
dgn-np:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_assertion
dcterms:description
"[The missing teeth in both patients are described in detail, and these data are compared with the dental anomalies observed in the only two other families with deletions of PAX9 and with the data available for 12 previously reported families carrying different types of PAX9 mutations.]. 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:18445003
;
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:NP799490.RA_an13Hj76UG2CT9hfvhz1Fik6uzwmnwMslTqzanyLeI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}