@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU
> .
@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:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_head
{
this:
np:hasAssertion
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_assertion
;
np:hasProvenance
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_provenance
;
np:hasPublicationInfo
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_assertion
a
np:Assertion
.
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_provenance
a
np:Provenance
.
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_assertion
{
miriam-gene:79577
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN4c9925b3001ca3feeda6b1a3255dafb1
sio:SIO_000628
miriam-gene:79577
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_provenance
{
dgn-np:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_assertion
dcterms:description
"[We performed parafibromin and cyclin D1 immunostaining and HRPT2 gene analysis using loss of heterozygosity studies and sequencing analysis in parathyroid specimens from 11 patients with carcinoma (eleven primary tumors, one skin, and four lung metastases), 22 with sporadic adenomas, and 4 with atypical adenomas.]. 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:17468190
;
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:NP376657.RAm5gZYHFrEWecL_uK3al-QXgCCt5NwdJKlWgYvRp8DbU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}