@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI
> .
@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:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_head
{
this:
np:hasAssertion
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_assertion
;
np:hasProvenance
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_provenance
;
np:hasPublicationInfo
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_assertion
a
np:Assertion
.
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_provenance
a
np:Provenance
.
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGNfc2129aefd5b3f81bae1fe673ff120fa
sio:SIO_000628
miriam-gene:5979
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_provenance
{
dgn-np:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_assertion
dcterms:description
"[Although RET mutations are common in hereditary MTC and can occur in some cases of sporadic MTC, knowledge of other molecular defects associated with the development of MTC should reveal new targets for therapy.]. 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:18084343
;
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:NP645564.RAkbezLikoqHn-3yBfpujIwJ7lAnYZe1SGfE6lcKwWhiI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:38+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" .
}