@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54
> .
@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:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_head
{
this:
np:hasAssertion
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_assertion
;
np:hasProvenance
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_provenance
;
np:hasPublicationInfo
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_assertion
a
np:Assertion
.
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_provenance
a
np:Provenance
.
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_assertion
{
miriam-gene:7428
a
ncit:C16612
.
lld:C0014132
a
ncit:C7057
.
dgn-gda:DGN131309e59785fb64a0dca9600e1dd77b
sio:SIO_000628
miriam-gene:7428
,
lld:C0014132
;
a
sio:SIO_001121
.
}
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_provenance
{
dgn-np:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_assertion
dcterms:description
"[We mapped the MenX locus to the distal part of rat chromosome 4, excluding the homologs of the genes responsible for the MEN syndromes (RET and MEN1) and syndromes with an endocrine tumor component (VHL and NF1).]. 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:17030811
;
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:NP823016.RA4OBIcuw1bBM-kjTk7QLid48BbFR4XIp_vNp5SPLnZ54130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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" .
}