@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk
> .
@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:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_head
{
this:
np:hasAssertion
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_assertion
;
np:hasProvenance
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_provenance
;
np:hasPublicationInfo
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_assertion
a
np:Assertion
.
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_provenance
a
np:Provenance
.
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_assertion
{
miriam-gene:1357
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN5ce5735174c5c70801cba1a6eeeac0ed
sio:SIO_000628
miriam-gene:1357
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_provenance
{
dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_assertion
dcterms:description
"[We have analyzed, using the mixed model, the whole sample of nonsyndromic CP, including isolated (i.e., without other anomalies) CP (CPI) and CP associated with at least one other anomaly (CPA), for which a diagnosis of malformation syndrome was not possible.]. 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:9254850
;
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:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}