@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w
> .
@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:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_head
{
this:
np:hasAssertion
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_assertion
;
np:hasProvenance
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_provenance
;
np:hasPublicationInfo
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_assertion
a
np:Assertion
.
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_provenance
a
np:Provenance
.
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_assertion
{
miriam-gene:2260
a
ncit:C16612
.
lld:C0162809
a
ncit:C7057
.
dgn-gda:DGN70f7c645ac530680e131d70311b27e6e
sio:SIO_000628
miriam-gene:2260
,
lld:C0162809
;
a
sio:SIO_001121
.
}
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_provenance
{
dgn-np:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_assertion
dcterms:description
"[Considering the low prevalence of mutations in KAL1 or FGFR1 in KS, it is possible that these genotypes are more prevalent in reversible KS than in other KS patients, but additional studies are necessary to confirm this hypothesis.]. 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:17322486
;
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:NP595841.RATpH96rB61jjFKgeoVWHuXVF8_81tmZKGVb1zXunBc4w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:15+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: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" .
}