@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_head
{
this:
np:hasAssertion
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion
;
np:hasProvenance
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance
;
np:hasPublicationInfo
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion
a
np:Assertion
.
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance
a
np:Provenance
.
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion
{
miriam-gene:3670
a
ncit:C16612
.
lld:C0018818
a
ncit:C7057
.
dgn-gda:DGN0af597c3ebeac403027a65767f5dc1c3
sio:SIO_000628
miriam-gene:3670
,
lld:C0018818
;
a
sio:SIO_001121
.
}
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_provenance
{
dgn-np:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_assertion
dcterms:description
"[ISL1 is related to the atrial septal defect group and the ventricular septal defect group, and the genotypes were associated with the occurrence of CHD in the dominant mode of inheritance.]. 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:24634231
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP516220.RAC2H8KRF9AVozTYE4eOYkb-T-k8qBwpp24OfT6WHy_Bs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:45+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}