@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA
> .
@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:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_head
{
this:
np:hasAssertion
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_assertion
;
np:hasProvenance
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_provenance
;
np:hasPublicationInfo
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_assertion
a
np:Assertion
.
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_provenance
a
np:Provenance
.
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_assertion
{
miriam-gene:6964
a
ncit:C16612
.
lld:C0005944
a
ncit:C7057
.
dgn-gda:DGN1aa5c5127c3e3d5c6933b161ca60fe5a
sio:SIO_000628
miriam-gene:6964
,
lld:C0005944
;
a
sio:SIO_001121
.
}
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_provenance
{
dgn-np:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_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:NP932955.RAU4w7XSrJK2r1YH5I2xNXAXvRxSiwtCaSfeuvd2Yf0aA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:32+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" .
}