@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE
> .
@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:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_head
{
this:
np:hasAssertion
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_assertion
;
np:hasProvenance
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_provenance
;
np:hasPublicationInfo
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_assertion
a
np:Assertion
.
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_provenance
a
np:Provenance
.
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_assertion
{
miriam-gene:2006
a
ncit:C16612
.
lld:C0243050
a
ncit:C7057
.
dgn-gda:DGN4c90ae8fb48781e8b0479d858ccf48d9
sio:SIO_000628
miriam-gene:2006
,
lld:C0243050
;
a
sio:SIO_001121
.
}
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_provenance
{
dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_assertion
dcterms:description
"[Molecular genetic studies have shown that deletion at the elastin gene may account for the cardiovascular abnormalities seen in WS, but autistic features are likely caused by other genes flanking elastin.]. 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:16861145
;
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:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}