@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8
> .
@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:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_head
{
this:
np:hasAssertion
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_assertion
;
np:hasProvenance
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_provenance
;
np:hasPublicationInfo
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_assertion
a
np:Assertion
.
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_provenance
a
np:Provenance
.
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_assertion
{
miriam-gene:2475
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGNefd548272928e4fcf445c121dc5e93d8
sio:SIO_000628
miriam-gene:2475
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_provenance
{
dgn-np:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_assertion
dcterms:description
"[In addition, the recent findings of H-RAS mutations in 56% of RET-negative sporadic MTC and the activation of the mammalian target of rapamycin (mTOR) intracellular signaling pathway in hereditary MTC suggests that additional or alternative genetic events are important for MTC pathogenesis.]. 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:22343387
;
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:NP845711.RAR6FDbFh3Gdf2zjcUER1uWkItfVpXOwVO6wo1huVRDn8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}