@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY
> .
@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:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_head
{
this:
np:hasAssertion
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_assertion
;
np:hasProvenance
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_provenance
;
np:hasPublicationInfo
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_assertion
a
np:Assertion
.
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_provenance
a
np:Provenance
.
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_assertion
{
miriam-gene:2006
a
ncit:C16612
.
lld:C0018798
a
ncit:C7057
.
dgn-gda:DGN8a6283d03213ea0e3a2b48e40bd0d895
sio:SIO_000628
miriam-gene:2006
,
lld:C0018798
;
a
sio:SIO_001121
.
}
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_provenance
{
dgn-np:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_assertion
dcterms:description
"[Molecular genetic studies have indicated that hemizygosity at the elastin locus (ELN) may account for the cardiac abnormalities seen in WS, but that mental retardation and hypercalcemia are likely caused by other genes flanking ELN.]. 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:9637430
;
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:NP276635.RAQAzKrWXQ40UqqZFA0whXWQmx2J3YYCFfrmu1MTVpFaY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}