@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M
> .
@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:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_head
{
this:
np:hasAssertion
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_assertion
;
np:hasProvenance
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_provenance
;
np:hasPublicationInfo
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_assertion
a
np:Assertion
.
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_provenance
a
np:Provenance
.
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0031511
a
ncit:C7057
.
dgn-gda:DGN2effde0c09abbf8a3ebe92a592ac691f
sio:SIO_000628
miriam-gene:4221
,
lld:C0031511
;
a
sio:SIO_001121
.
}
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_provenance
{
dgn-np:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_assertion
dcterms:description
"[Extension of the screening program can now be anticipated for other inherited forms of MTC, such as familial MTC without pheochromocytoma or other endocrinological tumor syndromes such as MEN1 for which the locus has also recently been mapped.]. 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:2575577
;
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:NP535424.RA53by2jxW7brqzJeTLEcMKCKIauHNr3rH-2HY0tUvJ_M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}