@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28
> .
@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:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_head
{
this:
np:hasAssertion
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_assertion
;
np:hasProvenance
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_provenance
;
np:hasPublicationInfo
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_assertion
a
np:Assertion
.
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_provenance
a
np:Provenance
.
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_assertion
{
miriam-gene:138428
a
ncit:C16612
.
lld:C0025267
a
ncit:C7057
.
dgn-gda:DGNca14c0cebea45ecc6954248b40986d25
sio:SIO_000628
miriam-gene:138428
,
lld:C0025267
;
a
sio:SIO_001121
.
}
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_provenance
{
dgn-np:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_assertion
dcterms:description
"[Analyses on tumor DNA from one case of PC and one of atypical adenoma showed no evidence of ras gene mutations, PTH gene rearrangement, or allelic loss from chromosome 11q13 (locus of the gene for multiple endocrine neoplasia type 1).]. 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:1639936
;
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:NP782964.RA3QTj7wOg6JhnIb9hpeuBc8ZHAQ69_3KOsl1oKLrxk28130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}