@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w
> .
@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/v3.0.0/void/
> .
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_head
{
this:
np:hasAssertion
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_assertion
;
np:hasProvenance
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_provenance
;
np:hasPublicationInfo
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_assertion
a
np:Assertion
.
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_provenance
a
np:Provenance
.
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_assertion
{
miriam-gene:8102
a
ncit:C16612
.
lld:C0007114
a
ncit:C7057
.
dgn-gda:DGNaf6767a1614ac1ea80ff00d9a86d69d9
sio:SIO_000628
miriam-gene:8102
,
lld:C0007114
;
a
sio:SIO_001121
.
}
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_provenance
{
dgn-np:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_assertion
dcterms:description
"[We have tested G2 chromosomal X-ray sensitivity in peripheral blood lymphocytes from members of kindreds with hereditary cutaneous malignant melanoma (HCMM) combined with the dysplastic nevus syndrome (DNS), disorders in which susceptibility to skin cancer is inherited in an autosomal dominant pattern.]. 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:10082912
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP790571.RAOi3G0Ht0_tSH6L-Ft78TI-1RmjDx_HOywwn9BHXbY-w130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:38+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}