@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo
> .
@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:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_head
{
this:
np:hasAssertion
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_assertion
;
np:hasProvenance
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_provenance
;
np:hasPublicationInfo
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_assertion
a
np:Assertion
.
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_provenance
a
np:Provenance
.
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_assertion
{
miriam-gene:5727
a
ncit:C16612
.
lld:C0812437
a
ncit:C7057
.
dgn-gda:DGNcbeca5401e376bc84171b6b1c77d3a49
sio:SIO_000628
miriam-gene:5727
,
lld:C0812437
;
a
sio:SIO_001121
.
}
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_provenance
{
dgn-np:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_assertion
dcterms:description
"[Unresolved complexities of the pathway impede understanding of mechanisms through which PTCH alterations lead to variable phenotype expression in Gorlin syndrome patients, while the role of chromosomal instability is not yet clear.]. 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:10653132
;
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:NP273698.RA-RPInIMtZyxpVE-cL7FAaWT9Gpp7kMpVlS2ldPcElKo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:50+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" .
}