@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo
> .
@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:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_head
{
this:
np:hasAssertion
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_assertion
;
np:hasProvenance
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_provenance
;
np:hasPublicationInfo
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_assertion
a
np:Assertion
.
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_provenance
a
np:Provenance
.
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNf68c189311a79b4bcdf20ed76ed6e9c2
sio:SIO_000628
miriam-gene:5979
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_provenance
{
dgn-np:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_assertion
dcterms:description
"[Although kidney agenesis or dysgenesis has been observed in mice lacking functional ret, no clinically relevant kidney abnormalities have been reported in individuals with known RET mutations and familial medullary thyroid carcinoma (FMTC).]. 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:11454140
;
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:NP526407.RAwhM9vrVHgUdAIF0gGMid6pZNRoxZjFCgqfwMWzcB6Qo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}