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http://rdf.disgenet.org/nanopublications.trig#NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_assertion
a
np:Assertion
.
dgn-np:NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance
a
np:Provenance
.
dgn-np:NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:8924
a
ncit:C16612
.
lld:C0575081
a
ncit:C7057
.
dgn-gda:DGN047c00d4d0ce6f44089b5aef8e1f489f
sio:SIO_000628
miriam-gene:8924
,
lld:C0575081
;
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.
}
dgn-np:NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_provenance
{
dgn-np:NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_assertion
dcterms:description
"[The phenotypic correlation with the mouse Herc1 and Herc2 mutants as well as the phenotypic overlap with Angelman syndrome provide further evidence that pathogenic changes in HERC2 are associated with nonsyndromic intellectual disability, autism, and gait disturbance.]. 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:23065719
;
prov:wasDerivedFrom
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;
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 .
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dgn-np:NP832067.RAicU1Gbrg0L-PsgV1Ezo2PuZzJrY_cJBmUTAkYZEzBFY130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
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> , <
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> , <
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> ;
pav:createdBy
<
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pav:version
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"v2.1.0" .
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