@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4
> .
@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:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_head
{
this:
np:hasAssertion
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_assertion
;
np:hasProvenance
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_provenance
;
np:hasPublicationInfo
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_assertion
a
np:Assertion
.
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_provenance
a
np:Provenance
.
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_assertion
{
miriam-gene:6095
a
ncit:C16612
.
lld:C0221357
a
ncit:C7057
.
dgn-gda:DGN322848950034fbae6e86ecd97697d29e
sio:SIO_000628
miriam-gene:6095
,
lld:C0221357
;
a
sio:SIO_001121
.
}
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_provenance
{
dgn-np:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_assertion
dcterms:description
"[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. 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:12011143
;
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:NP251640.RAiEAWR5oIRDLa0hWoXAHmYIqxyxwUm3DkoVnZtoBycc4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}