@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk
> .
@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:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_head
{
this:
np:hasAssertion
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_assertion
;
np:hasProvenance
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_provenance
;
np:hasPublicationInfo
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_assertion
a
np:Assertion
.
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_provenance
a
np:Provenance
.
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_assertion
{
miriam-gene:182
a
ncit:C16612
.
lld:C1956257
a
ncit:C7057
.
dgn-gda:DGN025887f06057aea24d71b526ee7ab094
sio:SIO_000628
miriam-gene:182
,
lld:C1956257
;
a
sio:SIO_001121
.
}
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_provenance
{
dgn-np:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_assertion
dcterms:description
"[Recent studies have implicated the Notch signaling pathway in human cardiac development by demonstrating abnormalities of the JAG1 gene as the basis for Alagille syndrome and some cases of isolated tetralogy of Fallot or pulmonic stenosis.]. 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:12372254
;
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:NP647324.RAx5Ca3abiJDR8ISr63af4csSXsHNVQx6wqJ94lOhr9qk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}