@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4
> .
@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:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_head
{
this:
np:hasAssertion
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_assertion
;
np:hasProvenance
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_provenance
;
np:hasPublicationInfo
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_assertion
a
np:Assertion
.
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_provenance
a
np:Provenance
.
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0027662
a
ncit:C7057
.
dgn-gda:DGN04f09bc8838b23a131e1cc7f79532619
sio:SIO_000628
miriam-gene:5979
,
lld:C0027662
;
a
sio:SIO_001121
.
}
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_provenance
{
dgn-np:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_assertion
dcterms:description
"[The aim of the present study is to detect the proportion of MTC cases having inherited germline or somatic RET mutations and to identify family members at risk for MEN and, thereby the feasibility of screening for MEN.]. 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:16758654
;
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:NP553457.RAOpLFNi99cSGi5_3Klv89L_vlaqTnnXFaRW5C5hQAYV4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:55+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" .
}