@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA
> .
@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:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_head
{
this:
np:hasAssertion
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_assertion
;
np:hasProvenance
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_provenance
;
np:hasPublicationInfo
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_assertion
a
np:Assertion
.
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_provenance
a
np:Provenance
.
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_assertion
{
miriam-gene:7864
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN821c0ef04baf035ec5d6d5e6d5474826
sio:SIO_000628
miriam-gene:7864
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_provenance
{
dgn-np:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_assertion
dcterms:description
"[Persons with this mutant gene should be at increased risk to develop SCLC, and further RFLP analysis of the 3p region in SCLC may allow identification of specific haplotypes with increased risk of developing lung cancer.]. 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:3472765
;
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:NP634563.RAYLJhsInNysyILA7P1DDjkEsH4kOUwd2XZ7YI_yByfnA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}