@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_head
{
this:
np:hasAssertion
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion
;
np:hasProvenance
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance
;
np:hasPublicationInfo
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion
a
np:Assertion
.
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance
a
np:Provenance
.
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0020502
a
ncit:C7057
.
dgn-gda:DGN9aeea99d1bbc94e73d43175991a93089
sio:SIO_000628
miriam-gene:4221
,
lld:C0020502
;
a
sio:SIO_001121
.
}
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_provenance
{
dgn-np:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_assertion
dcterms:description
"[We therefore suggest that routine germline MEN1 mutation testing of all cases of classical MEN1, familial hyperparathyroidism, and sporadic hyperparathyroidism with one other MEN1 related condition is justified by national testing services.]. 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:15635078
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP475136.RAS8s34RjeQIWFgs9DeVAIhSC_1O_x9tIBku8rrt0_ZvI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:20+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}