@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ
> .
@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:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_head
{
this:
np:hasAssertion
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_assertion
;
np:hasProvenance
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_assertion
a
np:Assertion
.
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_provenance
a
np:Provenance
.
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGN41a8589f06eb7a4ed71d5c9f9abb372b
sio:SIO_000628
miriam-gene:5979
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_provenance
{
dgn-np:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_assertion
dcterms:description
"[The dominantly inherited Multiple Endocrine Neoplasia cancer syndrome type 2B (MEN2B) is characterized by the presence of medullary thyroid carcinoma (MTC), phaechromocytoma (PHAEO), mucosal neuromas, ganglioneuromas of the intestinal tract, skeletal and ophthalmic abnormalities.]. 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:9700574
;
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:NP1401637.RAiQ3UIgDNsoLgeNClTnb6upUdYKnwkp3c_9ykcjuc9QQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:21+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" .
}