@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k
> .
@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:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_head
{
this:
np:hasAssertion
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_assertion
;
np:hasProvenance
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_provenance
;
np:hasPublicationInfo
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_assertion
a
np:Assertion
.
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_provenance
a
np:Provenance
.
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_assertion
{
miriam-gene:796
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGNf0358caf6ed89423642669abbc4e23d9
sio:SIO_000628
miriam-gene:796
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_provenance
{
dgn-np:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_assertion
dcterms:description
"[RET genotypes (exons 10, 11, 13, and 14) of 63 patients with hereditary MTC (from November 1994 to October 1999) were correlated with age at diagnosis, sex, the TNM system, and basal calcitonin levels.]. 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:11238493
;
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:NP310191.RAybFQHmglim_InpQVRAHQGxbB9HE9OctQSRGNpKf4E7k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:06+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" .
}