@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8
> .
@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:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_head
{
this:
np:hasAssertion
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_assertion
;
np:hasProvenance
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_provenance
;
np:hasPublicationInfo
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_assertion
a
np:Assertion
.
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_provenance
a
np:Provenance
.
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C1833921
a
ncit:C7057
.
dgn-gda:DGN2075c2ea97c51b99b29b0a8b8a684a81
sio:SIO_000628
miriam-gene:5979
,
lld:C1833921
;
a
sio:SIO_001121
.
}
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_provenance
{
dgn-np:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_assertion
dcterms:description
"[In multiple endocrine neoplasia type 2A (MEN 2A) and familial medullary thyroid cancer (FMTC), the majority of germline mutations are restricted to specific positions in exons 10 and 11 of the RET gene.]. 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:12694233
;
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:NP161910.RAC-oyfidAqAT0XHzVe21HsdVmH-Axm5A8OheamNG4oV8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}