@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM
> .
@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:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_head
{
this:
np:hasAssertion
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion
;
np:hasProvenance
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance
;
np:hasPublicationInfo
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion
a
np:Assertion
.
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance
a
np:Provenance
.
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion
{
miriam-gene:55349
a
ncit:C16612
.
lld:C0152021
a
ncit:C7057
.
dgn-gda:DGN023a0aadc6cc764c9c136f3401fcc2bd
sio:SIO_000628
miriam-gene:55349
,
lld:C0152021
;
a
sio:SIO_001121
.
}
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_provenance
{
dgn-np:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_assertion
dcterms:description
"[There is evidence suggesting that genetic variants of Nodal signaling may be associated with risk of congenital heart diseases (CHDs), in which several polymorphisms, such as Nodal rs1904589, have been considered to be implicated in the accumulation of the genetic burden of CHD risk with interacting genes.]. 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:23076529
;
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:NP535987.RAiAeVpMZQlIW5WbjN7z89uPpOqrSXy9ZEacy1BoQXNYM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}