@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE
> .
@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/v3.0.0/void/
> .
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_head
{
this:
np:hasAssertion
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_assertion
;
np:hasProvenance
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_provenance
;
np:hasPublicationInfo
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_assertion
a
np:Assertion
.
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_provenance
a
np:Provenance
.
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_assertion
{
miriam-gene:650
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN1b5c9d1a0ebf48a31437ab1544e3558d
sio:SIO_000628
miriam-gene:650
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_provenance
{
dgn-np:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_assertion
dcterms:description
"[In summary, our findings support the conclusions that BMP2 is the causing gene for BDA2, that the genomic location corresponding to the duplication region is prone to structural changes associated with malformation of the digits, and that this tendency is probably caused by the abundance of microhomologous sequences in the region.]. 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:24710560
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP268897.RAbqLADwHS3WDYw3HKWVS0kuY8GcQf0qltz3QRGCPSLcE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:13+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}