@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4
> .
@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:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_head
{
this:
np:hasAssertion
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_assertion
;
np:hasProvenance
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_provenance
;
np:hasPublicationInfo
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_assertion
a
np:Assertion
.
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_provenance
a
np:Provenance
.
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_assertion
{
miriam-gene:846
a
ncit:C16612
.
lld:C0025267
a
ncit:C7057
.
dgn-gda:DGNd9ac37cd14b6f877a7e47953593e462a
sio:SIO_000628
miriam-gene:846
,
lld:C0025267
;
a
sio:SIO_001121
.
}
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_provenance
{
dgn-np:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_assertion
dcterms:description
"[These include chromosomal deletions of the MEN1 locus on 11q in sporadic and MEN1 associated primary HPT, of RB1 on 13q in carcinomas, and of the FHH gene located on 3q in sporadic primary and secondary HPT.]. 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:8981014
;
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:NP203035.RAu7Bvl30GONBb8AE74OPpM1uG4EbmKwNtR1sHBjTewP4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}