@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34
> .
@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:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_head
{
this:
np:hasAssertion
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_assertion
;
np:hasProvenance
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_provenance
;
np:hasPublicationInfo
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_assertion
a
np:Assertion
.
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_provenance
a
np:Provenance
.
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_assertion
{
miriam-gene:9241
a
ncit:C16612
.
lld:C1969652
a
ncit:C7057
.
dgn-gda:DGN14f769470ef080dbcfc0cc47ce6e4ff6
sio:SIO_000628
miriam-gene:9241
,
lld:C1969652
;
a
sio:SIO_001121
.
}
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_provenance
{
dgn-np:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_assertion
dcterms:description
"[BDB1 is caused by mutations in the receptor tyrosine kinase gene ROR2, which maps to chromosome 9q22, whereas BDB2 is caused by point mutations in the bone morphogenetic protein antagonist NOGGIN.]. 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:24954533
;
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:NP1194759.RAU_z8AEKOj1nqniocaVfJEyCahUYQRSsry0apW1I7J34130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:47+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" .
}