@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc
> .
@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:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_head
{
this:
np:hasAssertion
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_assertion
;
np:hasProvenance
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_provenance
;
np:hasPublicationInfo
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_assertion
a
np:Assertion
.
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_provenance
a
np:Provenance
.
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_assertion
{
miriam-gene:7192
a
ncit:C16612
.
lld:C0005944
a
ncit:C7057
.
dgn-gda:DGN41d77a1c87731e3136d59ff7a2000829
sio:SIO_000628
miriam-gene:7192
,
lld:C0005944
;
a
sio:SIO_001121
.
}
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_provenance
{
dgn-np:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_assertion
dcterms:description
"[Nine of 10 recurrent mutations were located in either the methyl CpG binding domain (MBD) or in the transcriptional repression domain (TRD), and all missense mutations were located in one of these functionally important domains.]. 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:11241840
;
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:NP850504.RA2rPMN4JWzDoW9u_9unjJc9de3sH7pJ3nirUd02NLdAc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:40+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" .
}