@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE
> .
@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:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_head
{
this:
np:hasAssertion
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_assertion
;
np:hasProvenance
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_provenance
;
np:hasPublicationInfo
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_assertion
a
np:Assertion
.
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_provenance
a
np:Provenance
.
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_assertion
{
miriam-gene:2887
a
ncit:C16612
.
lld:C0025268
a
ncit:C7057
.
dgn-gda:DGN000652eb8c3af790f36712084a272fb2
sio:SIO_000628
miriam-gene:2887
,
lld:C0025268
;
a
sio:SIO_001121
.
}
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_provenance
{
dgn-np:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_assertion
dcterms:description
"[The gene for multiple endocrine neoplasia type 2A (MEN 2A) is closely linked to RBP3 (retinol-binding protein 3, interstitial, probe IRBP.H4) and the DNA marker D10S15 (probe pMCK2), which have been assigned to the proximal long arm of chromosome 10 by linkage analysis both in Caucasian and Japanese populations.]. 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:1982737
;
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:NP470478.RAnB1v_CHW0dmyOBwMHws1WMXwOHpok_QhfI-3-DQpDjE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}