@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4
> .
@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:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_head
{
this:
np:hasAssertion
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_assertion
;
np:hasProvenance
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_provenance
;
np:hasPublicationInfo
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_assertion
a
np:Assertion
.
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_provenance
a
np:Provenance
.
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_assertion
{
miriam-gene:1800
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNf0a12702fdd43c2c7a996b17138b6eeb
sio:SIO_000628
miriam-gene:1800
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_provenance
{
dgn-np:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_assertion
dcterms:description
"[Although our findings could not confirm that the genes of this family are responsible for the etiology in the majority of autistic patients, the R269C mutation in the MBD1 gene may relate to autism.]. 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:15967618
;
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:NP683986.RAgvBNMWiyKqxe-RQgeFQHzsSrWJZlC_lsuPqNwGrLfH4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}