@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY
> .
@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:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_head
{
this:
np:hasAssertion
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_assertion
;
np:hasProvenance
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_provenance
;
np:hasPublicationInfo
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_assertion
a
np:Assertion
.
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_provenance
a
np:Provenance
.
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_assertion
{
miriam-gene:8102
a
ncit:C16612
.
lld:C0013403
a
ncit:C7057
.
dgn-gda:DGN4a0e3173e0ff6cc49c0083c8280513ac
sio:SIO_000628
miriam-gene:8102
,
lld:C0013403
;
a
sio:SIO_001121
.
}
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_provenance
{
dgn-np:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_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:NP790572.RAJZCIlAt6zQSTHGYgfTwOcpfqfnK9iJ-PQSiSZwkhktY130_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" .
}