@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls
> .
@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:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_head
{
this:
np:hasAssertion
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_assertion
;
np:hasProvenance
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_provenance
;
np:hasPublicationInfo
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_assertion
a
np:Assertion
.
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_provenance
a
np:Provenance
.
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C3489630
a
ncit:C7057
.
dgn-gda:DGN563af1c53b69a78f780a23e6b1b4184b
sio:SIO_000628
miriam-gene:4221
,
lld:C3489630
;
a
sio:SIO_001121
.
}
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_provenance
{
dgn-np:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_assertion
dcterms:description
"[Although mutations in the promoter, introns or untranslated regions of the MEN1 gene cannot be excluded, germline mutations within the coding region of this gene do not appear responsible for IFS in this family.]. 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:12638720
;
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:NP802749.RAhpu7T0rTdFT9toTAqYY8gfhfyecGdN0WY7b0kpce2Ls130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}