@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0
> .
@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:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_head
{
this:
np:hasAssertion
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_assertion
;
np:hasProvenance
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_provenance
;
np:hasPublicationInfo
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_assertion
a
np:Assertion
.
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_provenance
a
np:Provenance
.
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_assertion
{
miriam-gene:2006
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGNc8b7b6764a0c03c5bf15a1a7c146cc71
sio:SIO_000628
miriam-gene:2006
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_provenance
{
dgn-np:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_assertion
dcterms:description
"[Characterization of the molecular basis of structural cardiac disease includes elucidating the pathogenesis of certain vascular disease by demonstrating mutations of the Elastin gene as the cause of familial supravalvular aortic stenosis (SVAS) and Williams' syndrome (WS).]. 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:9986885
;
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:NP311834.RA40IA2VozGclru1VnwaZaVYvQxfUSzZ_-8v3StZeTcy0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}