@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8
> .
@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:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_head
{
this:
np:hasAssertion
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_assertion
;
np:hasProvenance
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_provenance
;
np:hasPublicationInfo
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_assertion
a
np:Assertion
.
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_provenance
a
np:Provenance
.
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_assertion
{
miriam-gene:1869
a
ncit:C16612
.
lld:C0030521
a
ncit:C7057
.
dgn-gda:DGN438bd5407ad1e9323d5786cf84c4c713
sio:SIO_000628
miriam-gene:1869
,
lld:C0030521
;
a
sio:SIO_001121
.
}
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_provenance
{
dgn-np:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_assertion
dcterms:description
"[Furthermore, the locus that codes for a distinct phenotype, medullary thyroid carcinoma (MTC) with parathyroid tumors (PTs) and no pheochromocytomas (PHEOs) (referred to as MTC with PTs), in one of the families was closely linked to two markers, D10Z1 and RBP3, with lodscores of 2.86 and 3.54, respectively, at theta = 0.]. 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:1978560
;
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:NP739541.RAYEOewHUte8Um9BVgbgJ7oNaL7lJjtwYujoMNZ_fW2F8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:28+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" .
}