@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y
> .
@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:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_head
{
this:
np:hasAssertion
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_assertion
;
np:hasProvenance
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_assertion
a
np:Assertion
.
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_provenance
a
np:Provenance
.
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_assertion
{
miriam-gene:2294
a
ncit:C16612
.
lld:C0221210
a
ncit:C7057
.
dgn-gda:DGNf20eff4be358c2d82fddbc233204fc6d
sio:SIO_000628
miriam-gene:2294
,
lld:C0221210
;
a
sio:SIO_001121
.
}
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_provenance
{
dgn-np:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_assertion
dcterms:description
"[In many instances, recognition of a specific syndrome is possible, one of several examples discussed being the recently described association of intestinal malrotation with alveolar capillary dysplasia, due to mutations in the forkhead box transcription factor FOXF1.]. 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:20549505
;
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:NP895800.RAkyIu8lCmDwee6hZbmRgs9ozufffpgeUjAWsJOe48-3Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:10+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" .
}