@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4
> .
@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:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_head
{
this:
np:hasAssertion
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_assertion
;
np:hasProvenance
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_provenance
;
np:hasPublicationInfo
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_assertion
a
np:Assertion
.
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_provenance
a
np:Provenance
.
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN4a5226e7b3b1674c76c5331b7a1ae848
sio:SIO_000628
miriam-gene:4204
,
lld:C0035372
;
a
sio:SIO_001122
.
}
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_provenance
{
dgn-np:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_assertion
dcterms:description
"[The International Rett Syndrome Association (IRSA) North American database is the first comprehensive compilation of information in the United States and Canada on individuals with Rett syndrome or another diagnosis in association with MECP2 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:18174548
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP136860.RAubARM3auOxAaXk53R2SF_J4NXKpt_MM0gimhDkxdRp4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:11+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" .
}