@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU
> .
@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:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_head
{
this:
np:hasAssertion
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_assertion
;
np:hasProvenance
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_provenance
;
np:hasPublicationInfo
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_assertion
a
np:Assertion
.
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_provenance
a
np:Provenance
.
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_assertion
{
miriam-gene:2304
a
ncit:C16612
.
lld:C0008924
a
ncit:C7057
.
dgn-gda:DGN07b33148207ba0956be5f08b96e67183
sio:SIO_000628
miriam-gene:2304
,
lld:C0008924
;
a
sio:SIO_001121
.
}
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_provenance
{
dgn-np:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_assertion
dcterms:description
"[Further, results were phenotype dependent in that the IRF6 region results were most significant for families in which affected individuals have CL alone, and the FOXE1 region results were most significant in families in which some or all of the affected individuals have CL with CP.]. 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:19521098
;
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:NP503146.RALTLT2jhZZvSzod4jUmsCeGohVSyZTENcpQia0PLWblU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}