@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E
> .
@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:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_head
{
this:
np:hasAssertion
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_assertion
;
np:hasProvenance
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_provenance
;
np:hasPublicationInfo
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_assertion
a
np:Assertion
.
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_provenance
a
np:Provenance
.
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0677607
a
ncit:C7057
.
dgn-gda:DGN8a63c65158c91162adf47aa0430fe0b9
sio:SIO_000628
miriam-gene:7157
,
lld:C0677607
;
a
sio:SIO_001121
.
}
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_provenance
{
dgn-np:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_assertion
dcterms:description
"[With respect to allelic analysis, we did not observe significant difference in the frequency of appearance of the Arg allelic variant and the Pro allelic variant for the p53 codon 72 when comparing the HT patient group with the control group (P=0.208).]. 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:18803266
;
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:NP753464.RA7g8zJraxUmzi1S4DbUo7AK6LPp0Wr71ajigWB9GJv0E130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:14+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" .
}