@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c
> .
@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:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_head
{
this:
np:hasAssertion
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_assertion
;
np:hasProvenance
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_provenance
;
np:hasPublicationInfo
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_assertion
a
np:Assertion
.
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_provenance
a
np:Provenance
.
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_assertion
{
miriam-gene:412
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNc4df90369d72a6c52fc29c12d36704a1
sio:SIO_000628
miriam-gene:412
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_provenance
{
dgn-np:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_assertion
dcterms:description
"[Using a 2.4 kb cDNA clone, expression of human STS was undetectable by Northern hybridization, but STS RNA was detected in human placenta, human breast cancer samples, and in breast carcinoma cell lines following reverse transcriptase-PCR amplification, using specific primers to yield a product of 472 bp.]. 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:8664167
;
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:NP505620.RAIVZAzHD_NXC-Ljq1IfL5abVakJwdY58REv5wDkexE9c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:01+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" .
}