@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE
> .
@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:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_head
{
this:
np:hasAssertion
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_assertion
;
np:hasProvenance
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_provenance
;
np:hasPublicationInfo
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_assertion
a
np:Assertion
.
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_provenance
a
np:Provenance
.
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_assertion
{
miriam-gene:10117
a
ncit:C16612
.
lld:C0266061
a
ncit:C7057
.
dgn-gda:DGN12f0f0b1624e58cfa763732478c08b15
sio:SIO_000628
miriam-gene:10117
,
lld:C0266061
;
a
sio:SIO_001121
.
}
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_provenance
{
dgn-np:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_assertion
dcterms:description
"[Open bite malocclusion occurred in individuals with AI caused by mutations in the AMELX and ENAM genes even though these genes are considered to be predominantly or exclusively expressed in teeth.]. 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:15892947
;
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:NP780733.RA0aerIqZPPn9uXMoj6VRayB1X5hpwiPTZa8TqZg69eQE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}