@prefix bfo: <
http://purl.obolibrary.org/obo/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE
> .
@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 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:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_head
{
this:
np:hasAssertion
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_assertion
;
np:hasProvenance
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_provenance
;
np:hasPublicationInfo
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_assertion
a
np:Assertion
.
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_provenance
a
np:Provenance
.
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_assertion
{
miriam-gene:100528024
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNc2df2f95206788e9facfa2922cc1875f
sio:SIO_000628
miriam-gene:100528024
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_provenance
{
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_assertion
dcterms:description
"[Using 11 DNA markers covering the entire distal region of 11p13, including the WAGR region, we have carried out molecular studies on 58 patients with one or more features of this syndrome and patients with other diseases or structural cytogenetic abnormalities associated with 11p13.]. 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:1769647
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
bfo:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
bfo:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:28+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" .
}