@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0
> .
@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:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_head
{
this:
np:hasAssertion
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_assertion
;
np:hasProvenance
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_provenance
;
np:hasPublicationInfo
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_assertion
a
np:Assertion
.
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_provenance
a
np:Provenance
.
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_assertion
{
miriam-gene:302
a
ncit:C16612
.
lld:C0025268
a
ncit:C7057
.
dgn-gda:DGNfd8da50705f3c477c4da8f542a11517b
sio:SIO_000628
miriam-gene:302
,
lld:C0025268
;
a
sio:SIO_001121
.
}
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_provenance
{
dgn-np:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_assertion
dcterms:description
"[Therefore, we suggest that MEN 2A families should not be subclassified into MEN 2A and FMTC, but rather according to their specific mutation in the RET protein (i.e., for this family MEN 2A RET C618S).]. 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:9003111
;
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:NP833852.RAxpZERmZpQ5NRGjk3h0KZeZpgvYoKQt2xJv7ujqZZnn0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}