@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk
> .
@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:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_head
{
this:
np:hasAssertion
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_assertion
;
np:hasProvenance
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_provenance
;
np:hasPublicationInfo
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_assertion
a
np:Assertion
.
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_provenance
a
np:Provenance
.
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_assertion
{
miriam-gene:404672
a
ncit:C16612
.
lld:C0037268
a
ncit:C7057
.
dgn-gda:DGN513ab573616ff40a88149941337bbe19
sio:SIO_000628
miriam-gene:404672
,
lld:C0037268
;
a
sio:SIO_001121
.
}
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_provenance
{
dgn-np:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_assertion
dcterms:description
"[Because the clinical phenotypes of these patients do not obviously differ from those of TTDs with mutations at other sites, we conclude that the lack of skin abnormalities in TTD is independent of the defective cellular responses to UV.]. 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:10667598
;
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:NP271118.RAGPpD3iitkYLMJzHI-HhdVvUSfJQR24M7XlbxzXPADAk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:31+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" .
}