@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s
> .
@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:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_head
{
this:
np:hasAssertion
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_assertion
;
np:hasProvenance
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_assertion
a
np:Assertion
.
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_provenance
a
np:Provenance
.
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C2939420
a
ncit:C7057
.
dgn-gda:DGN9ae279efb48972016e139e0162507de0
sio:SIO_000628
miriam-gene:5979
,
lld:C2939420
;
a
sio:SIO_001121
.
}
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_provenance
{
dgn-np:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_assertion
dcterms:description
"[The recognition of RET proto-oncogene mutations by genetic sequencing has allowed us to differentiate hereditary from sporadic MTC, so that it is now possible to identify and treat children at risk for this disease before development of metastasis.]. 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:18502338
;
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:NP644181.RA0z8rhu2M2l1GKvk99DGCv9aQzujulljnrXkxDvOGR0s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}