@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo
> .
@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:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_head
{
this:
np:hasAssertion
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_assertion
;
np:hasProvenance
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_provenance
;
np:hasPublicationInfo
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_assertion
a
np:Assertion
.
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_provenance
a
np:Provenance
.
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_assertion
{
miriam-gene:29974
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNf9bdb197204b1aa0d16347606f58d18a
sio:SIO_000628
miriam-gene:29974
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_provenance
{
dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_assertion
dcterms:description
"[The present report describes a case with cardiofacial syndrome and ACF associated other congenital anomalies, and provides criteria for differentiating absence of the depressor anguli oris muscle (DAOM) from palsy of the seventh cranial nerve and its central connections.]. 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:8741317
;
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:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}