@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE
> .
@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:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_head
{
this:
np:hasAssertion
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_assertion
;
np:hasProvenance
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_provenance
;
np:hasPublicationInfo
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_assertion
a
np:Assertion
.
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_provenance
a
np:Provenance
.
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_assertion
{
miriam-gene:51360
a
ncit:C16612
.
lld:C0020757
a
ncit:C7057
.
dgn-gda:DGNd4fb767506b52b25074ff1dc6ded75ae
sio:SIO_000628
miriam-gene:51360
,
lld:C0020757
;
a
sio:SIO_001121
.
}
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_provenance
{
dgn-np:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_assertion
dcterms:description
"[Since all patients with BRESEK/BRESHECK syndrome are male, and X-linked syndrome of ichthyosis follicularis with atrichia and photophobia is sometimes associated with several features of BRESEK/BRESHECK syndrome such as intellectual disability, vertebral and renal anomalies, and Hirschsprung disease, we analyzed the causal gene of ichthyosis follicularis with atrichia and photophobia syndrome, MBTPS2, in the present patient and identified an p.Arg429His mutation.]. 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:22105905
;
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:NP342683.RAIOOUY37-ol3QMH3CeK11lS9gA7PB59bDApY1T6v0LUE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:21+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" .
}