@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g
> .
@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:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_head
{
this:
np:hasAssertion
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_assertion
;
np:hasProvenance
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_assertion
a
np:Assertion
.
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_provenance
a
np:Provenance
.
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0025268
a
ncit:C7057
.
dgn-gda:DGN1c1ab3fd19bc46837bf0391c91cb924a
sio:SIO_000628
miriam-gene:5979
,
lld:C0025268
;
a
sio:SIO_001121
.
}
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_provenance
{
dgn-np:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_assertion
dcterms:description
"[Data derived from our series helped elucidate the role of RET genetic screening for the identification of all forms of MEN 2, and especially for FMTC, which are frequently clinically misdiagnosed as nonheritable, sporadic cases.]. 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:17895320
;
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:NP631845.RAmJO-QiXznrdtQz9yfPXn80MX0AgB6SzrY3nlGlbLj4g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:32+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" .
}