@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA
> .
@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:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_head
{
this:
np:hasAssertion
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_assertion
;
np:hasProvenance
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_provenance
;
np:hasPublicationInfo
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_assertion
a
np:Assertion
.
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_provenance
a
np:Provenance
.
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_assertion
{
miriam-gene:4914
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGNb245b1422ce0e0703c340b712db2571e
sio:SIO_000628
miriam-gene:4914
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_provenance
{
dgn-np:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_assertion
dcterms:description
"[In spite of the increasing number of variants being described in MTC, it appears that there is no direct clinical benefit in extending RET germ line analysis beyond the hot spot regions in sMTC.]. 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:22648435
;
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:NP295388.RAwCDg_G9R1qC4Ai_gly6XMzBCE4IO85PMuYSlIamLOuA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}