@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw
> .
@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:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_head
{
this:
np:hasAssertion
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_assertion
;
np:hasProvenance
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_provenance
;
np:hasPublicationInfo
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_assertion
a
np:Assertion
.
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_provenance
a
np:Provenance
.
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_assertion
{
miriam-gene:6418
a
ncit:C16612
.
lld:C0025990
a
ncit:C7057
.
dgn-gda:DGN75e1011dc50d0bbd20c41363d4ad25ab
sio:SIO_000628
miriam-gene:6418
,
lld:C0025990
;
a
sio:SIO_001121
.
}
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_provenance
{
dgn-np:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_assertion
dcterms:description
"[This comprehensive approach to expression profiling gives insights into the early development of the craniofacial region and provides markers for developmental structures and candidate genes, including SET and CCT3, for diseases such as orofacial clefting and micrognathia.]. 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:15703188
;
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:NP513236.RAyE0ySt_Y2kEoU6_iNnGImcxYu0j8kSTFM1oBjeX0MZw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}