@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA
> .
@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:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_head
{
this:
np:hasAssertion
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_assertion
;
np:hasProvenance
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_provenance
;
np:hasPublicationInfo
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_assertion
a
np:Assertion
.
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_provenance
a
np:Provenance
.
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_assertion
{
miriam-gene:1896
a
ncit:C16612
.
lld:C0013575
a
ncit:C7057
.
dgn-gda:DGN21632b0e1e68fc1930213d6939c4757c
sio:SIO_000628
miriam-gene:1896
,
lld:C0013575
;
a
sio:SIO_001121
.
}
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_provenance
{
dgn-np:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_assertion
dcterms:description
"[Mutations in the human ectodysplasin-A (EDA) are responsible for the most common form of the ectodermal dysplasia and the defective orthologous gene in mice produces the tabby phenotype, suggesting its vital role in the development of hair, sweat glands and 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:11751679
;
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:NP821919.RAfOWT6yRRhjeebXIJsIUv7kA7ogkqNzFvLe3zYUF4qNA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}