@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA
> .
@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:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_head
{
this:
np:hasAssertion
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_assertion
;
np:hasProvenance
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_assertion
a
np:Assertion
.
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_provenance
a
np:Provenance
.
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_assertion
{
miriam-gene:5727
a
ncit:C16612
.
lld:C3811653
a
ncit:C7057
.
dgn-gda:DGN823e73efec0ff3464b98adef5a49fd44
sio:SIO_000628
miriam-gene:5727
,
lld:C3811653
;
a
sio:SIO_001122
.
}
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_provenance
{
dgn-np:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_assertion
dcterms:description
"[In addition to those that are potential germline polymorphisms, we found three SMO missense mutations, and one PTCH1 frameshift mutation that are novel and have not been documented in basal cell carcinoma.]. 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:23349881
;
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:NP1047114.RA3tKd-bZyZkJe4KvgHu6mRT3_zTMXafFqQgJNbX7_ndA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:40+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" .
}