@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo
> .
@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:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_head
{
this:
np:hasAssertion
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_assertion
;
np:hasProvenance
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_provenance
;
np:hasPublicationInfo
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_assertion
a
np:Assertion
.
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_provenance
a
np:Provenance
.
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0085390
a
ncit:C7057
.
dgn-gda:DGN2acf9f49de07d19d653d700c1482b50c
sio:SIO_000628
miriam-gene:5925
,
lld:C0085390
;
a
sio:SIO_001121
.
}
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_provenance
{
dgn-np:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_assertion
dcterms:description
"[The affected individual has developed multiple independent benign and malignant tumours (tricholemmoma of the scalp, multiple trichoepitheliomata of the face, osteosarcoma of the ovary, bilateral breast cancer, malignant fibrous histiocytoma of the thigh and endometrial adenocarcinoma) and belongs to a family with some, but not all, features of the Li-Fraumeni syndrome.]. 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:8479749
;
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:NP906927.RAOyr2xXMX0cnnVa_oBn_QW76xmlnKLdCfTBRIP8sBvBo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:17+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" .
}