@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM
> .
@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:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_head
{
this:
np:hasAssertion
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_assertion
;
np:hasProvenance
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_provenance
;
np:hasPublicationInfo
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_assertion
a
np:Assertion
.
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_provenance
a
np:Provenance
.
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_assertion
{
miriam-gene:10036
a
ncit:C16612
.
lld:C0795907
a
ncit:C7057
.
dgn-gda:DGN016bf71cabe92e010e47abd846095157
sio:SIO_000628
miriam-gene:10036
,
lld:C0795907
;
a
sio:SIO_001121
.
}
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_provenance
{
dgn-np:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_assertion
dcterms:description
"[To investigate molecular and clinical aspects of conotruncal anomaly face (CAF), we studied the correlation between deletion size and phenotype and the mode of inheritance in 183 conotruncal anomaly face syndrome (CAFS) patients.]. 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:9737780
;
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:NP809654.RAeIciXY5Uo8BLoX6b_n1J0nhgL4zWsRXulMzp9EAnpQM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}