@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss
> .
@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:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_head
{
this:
np:hasAssertion
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_assertion
;
np:hasProvenance
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_provenance
;
np:hasPublicationInfo
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_assertion
a
np:Assertion
.
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_provenance
a
np:Provenance
.
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0025268
a
ncit:C7057
.
dgn-gda:DGNfe74ce43fe848448ae3f414eac29ae1e
sio:SIO_000628
miriam-gene:5979
,
lld:C0025268
;
a
sio:SIO_001121
.
}
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_provenance
{
dgn-np:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_assertion
dcterms:description
"[The two main phenotypes of the MEN 2 syndrome, known as MEN 2A and MEN 2B, are associated with different mutations of the RET oncogene, mostly located on exons 10 or 11 in MEN 2A and in codon 918 of exon 16 in MEN 2B.]. 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:15077909
;
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:NP439455.RA8qgsBqgsneQv6mGh-3M7Fqx_ot4l_qNsdWbBKMVuNss130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:04+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" .
}