@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw
> .
@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:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_head
{
this:
np:hasAssertion
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_assertion
;
np:hasProvenance
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_provenance
;
np:hasPublicationInfo
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_assertion
a
np:Assertion
.
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_provenance
a
np:Provenance
.
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGN918447322b0cca82a73ac55c35f107ab
sio:SIO_000628
miriam-gene:5979
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_provenance
{
dgn-np:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_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-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:NP673065.RAqS_oO-M0B_qK7UWIu3TpeUE5m2pcq8s1aHoBuOpTXgw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:50+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" .
}