@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs
> .
@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:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_head
{
this:
np:hasAssertion
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_assertion
;
np:hasProvenance
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_provenance
;
np:hasPublicationInfo
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_assertion
a
np:Assertion
.
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_provenance
a
np:Provenance
.
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_assertion
{
miriam-gene:139818
a
ncit:C16612
.
lld:C0025269
a
ncit:C7057
.
dgn-gda:DGN84f723f6e92ce6b6a26390391d3d6915
sio:SIO_000628
miriam-gene:139818
,
lld:C0025269
;
a
sio:SIO_001121
.
}
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_provenance
{
dgn-np:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_assertion
dcterms:description
"[The most important mutation associated with Multiple Endocrine Neoplasia type 2B (MEN 2B) is the change of thymine to cytosine in codon 918 of exon 16 in the RET oncogene (ATG → ACG).]. 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:21253810
;
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:NP972851.RA1dNL6YJX4q53jfqPVvr3rsgOKM4D263CqfD-sE8MLPs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:34+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" .
}