@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_assertion
a
np:Assertion
.
dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_provenance
a
np:Provenance
.
dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0020502
a
ncit:C7057
.
dgn-gda:DGNb7e59f7e6695ffa61ca5746ae8f0e30b
sio:SIO_000628
miriam-gene:4221
,
lld:C0020502
;
a
sio:SIO_001122
.
}
dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_provenance
{
dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_assertion
dcterms:description
"[These findings strongly favour a recommendation for MEN1 and CASR genotyping of patients with multiglandular FIHP, irrespective of urinary calcium excretion. However, it appears that HRPT2 genotyping should be reserved for cases in which other features of]. 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:14985373
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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 .
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dgn-np:NP84005.RAicnRWnrsQDGMaseGsRVhRy8IklJOQkIaU4fwdZTKHfM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:26+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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" .
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pav:version
"v4.0.0" .
}