@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE
> .
@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:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_head
{
this:
np:hasAssertion
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_assertion
;
np:hasProvenance
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_provenance
;
np:hasPublicationInfo
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_assertion
a
np:Assertion
.
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_provenance
a
np:Provenance
.
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_assertion
{
miriam-gene:8048
a
ncit:C16612
.
lld:C0158646
a
ncit:C7057
.
dgn-gda:DGN3f3d264c093148ad345032ac6d66f5cb
sio:SIO_000628
miriam-gene:8048
,
lld:C0158646
;
a
sio:SIO_001121
.
}
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_provenance
{
dgn-np:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_assertion
dcterms:description
"[Combining the results of chromosomal linkage studies of unidentified human CLP genes with insights from the mouse models, the following previously unexamined genes are identified as strong candidate genes for causative roles in human nonsyndromic CLP: BMP4, BMPR1B, TFAP2A, SOX4, WNT9B, WNT3, and SP8.]. 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:18181213
;
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:NP912995.RAIdBShd4iRvNBZW5RzfJ798rsO83xxv4wwr0mSHk2otE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}