@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ
> .
@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:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_head
{
this:
np:hasAssertion
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_assertion
;
np:hasProvenance
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_assertion
a
np:Assertion
.
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_provenance
a
np:Provenance
.
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGNb1ba063a8fdcf741d2546a2c56304136
sio:SIO_000628
miriam-gene:5979
,
lld:C0549473
;
a
sio:SIO_001121
.
}
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_provenance
{
dgn-np:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_assertion
dcterms:description
"[A deeper understanding of the molecular signaling of normal versus abnormal RET activity in cancer will enable the development of potential new treatments for patients with sporadic and inherited thyroid cancer or MEN 2 syndrome.]. 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:15982921
;
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:NP501244.RAdguqbSEkTMYoYD54QjyXMF6FqE2wz8Gl3kds6p6Z5jQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:32+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" .
}