@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI
> .
@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:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_head
{
this:
np:hasAssertion
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_assertion
;
np:hasProvenance
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_provenance
;
np:hasPublicationInfo
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_assertion
a
np:Assertion
.
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_provenance
a
np:Provenance
.
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0030521
a
ncit:C7057
.
dgn-gda:DGN97d775c3278d668970b799ed36c69fe8
sio:SIO_000628
miriam-gene:4221
,
lld:C0030521
;
a
sio:SIO_001121
.
}
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_provenance
{
dgn-np:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_assertion
dcterms:description
"[These data suggest that RET gene mutation may not be involved in the development of sporadic parathyroid tumors and hyperplasia secondary to uremia and that MEN1 gene mutation may not be or is rarely associated with development of parathyroid hyperplasia in MEN2A patients.]. 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:10915003
;
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:NP360952.RAsztmKqQPkBu0zyCwe_bH5dKnHf83fEC_iGvy6R8GQaI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
}