@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY
> .
@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:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_head
{
this:
np:hasAssertion
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_assertion
;
np:hasProvenance
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_provenance
;
np:hasPublicationInfo
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_assertion
a
np:Assertion
.
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_provenance
a
np:Provenance
.
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_assertion
{
miriam-gene:4487
a
ncit:C16612
.
lld:C0008925
a
ncit:C7057
.
dgn-gda:DGN716b46eb8fb568061135431af61bb784
sio:SIO_000628
miriam-gene:4487
,
lld:C0008925
;
a
sio:SIO_001122
.
}
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_provenance
{
dgn-np:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_assertion
dcterms:description
"[results are consistent with evidence from other studies in the US and Chile and confirm the importance of the MSX1 genotype in determining the risk of cleft lip with or without palate and cleft palate in Koreans ]. 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:17326252
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP143574.RA08HH6OQ3bgOv9BjbFLnpxzaIxVyErnnlumwelpJz2lY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:15+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" .
}