@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ
> .
@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:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_head
{
this:
np:hasAssertion
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_assertion
;
np:hasProvenance
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_assertion
a
np:Assertion
.
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_provenance
a
np:Provenance
.
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_assertion
{
miriam-gene:2201
a
ncit:C16612
.
lld:C0238669
a
ncit:C7057
.
dgn-gda:DGN2acd859d602daf6dfaffa13e9d8f839f
sio:SIO_000628
miriam-gene:2201
,
lld:C0238669
;
a
sio:SIO_001121
.
}
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_provenance
{
dgn-np:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_assertion
dcterms:description
"[Furthermore, analysis of the clinical data of the CCA patients with characterized FBN2 mutation indicate that CCA patients have aortic root dilatation and the vast majority lack evidence of congenital heart disease.]. 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:11754102
;
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:NP669528.RANrxihjR78HOTOSvPEZ4Dp10bG68o4YJ20Ow5WKEOCAQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}