@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I
> .
@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:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_head
{
this:
np:hasAssertion
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_assertion
;
np:hasProvenance
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_provenance
;
np:hasPublicationInfo
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_assertion
a
np:Assertion
.
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_provenance
a
np:Provenance
.
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_assertion
{
miriam-gene:652
a
ncit:C16612
.
lld:C0152427
a
ncit:C7057
.
dgn-gda:DGN0ca5fda167dc93b12bafd87f49cd21a8
sio:SIO_000628
miriam-gene:652
,
lld:C0152427
;
a
sio:SIO_001121
.
}
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_provenance
{
dgn-np:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_assertion
dcterms:description
"[It was previously reported that the BMP family was correlated with the morphogenesis of digits and ocular development, and Bmp4 heterozygous null mice revealed skeletal abnormalities including polydactyly and ocular anterior segment abnormalities.]. 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:18925664
;
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:NP263607.RAXmqGMvuvT8NMI-gAZgBZORBUGXcqfeFZucLVmeC4Q5I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}