@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_head
{
this:
np:hasAssertion
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_assertion
;
np:hasProvenance
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_provenance
;
np:hasPublicationInfo
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_assertion
a
np:Assertion
.
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_provenance
a
np:Provenance
.
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_assertion
{
miriam-gene:3664
a
ncit:C16612
.
lld:C0008925
a
ncit:C7057
.
dgn-gda:DGN20337567e006eb404a819ff9982e329a
sio:SIO_000628
miriam-gene:3664
,
lld:C0008925
;
a
sio:SIO_001121
.
}
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_provenance
{
dgn-np:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP744867.RAqw_Y9Rj6a3sD-S4XNGMUHDMa47I53KQNzLMfW6Decds130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:22+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}