@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk
> .
@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:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_head
{
this:
np:hasAssertion
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_assertion
;
np:hasProvenance
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_provenance
;
np:hasPublicationInfo
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_assertion
a
np:Assertion
.
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_provenance
a
np:Provenance
.
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_assertion
{
miriam-gene:5921
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNf118e7f69f8237597ece2cb0c2ab2eb4
sio:SIO_000628
miriam-gene:5921
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_provenance
{
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_assertion
dcterms:description
"[While for most human solid tumors genetic alterations of few distinct genetic regions have been found, studies on basal cell carcinomas (BCC) have shown the prevalence of several abnormalities including alterations of the three ras genes, GAP (GTPase activating protein), p53, PTCH (the human homologue of Drosophila patched) and SMOH (the human homologue of Drosophila smoothened).]. 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:11752813
;
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:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:48+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" .
}