@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0
> .
@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/v3.0.0/void/
> .
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_head
{
this:
np:hasAssertion
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_assertion
;
np:hasProvenance
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_provenance
;
np:hasPublicationInfo
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_assertion
a
np:Assertion
.
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_provenance
a
np:Provenance
.
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0019829
a
ncit:C7057
.
dgn-gda:DGNd24e903d0147d41de8a5ee5beb27f50f
sio:SIO_000628
miriam-gene:5979
,
lld:C0019829
;
a
sio:SIO_001121
.
}
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_provenance
{
dgn-np:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_assertion
dcterms:description
"[Results showed the benefit of systematic RET mutation screening in HD patients in order to identify the risk of MTC in preclinical stage of the disease in patients with HD and their family members.]. 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:17021738
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP670689.RAwgR5SJV0iFT7HnT5dYv_kVky15-DBDbZU2uMVxJwju0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:23+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}