@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw
> .
@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:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_head
{
this:
np:hasAssertion
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_assertion
;
np:hasProvenance
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_provenance
;
np:hasPublicationInfo
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_assertion
a
np:Assertion
.
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_provenance
a
np:Provenance
.
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_assertion
{
miriam-gene:11186
a
ncit:C16612
.
lld:C0280100
a
ncit:C7057
.
dgn-gda:DGN170fb315b5cb130e95cc2a9bf08457f4
sio:SIO_000628
miriam-gene:11186
,
lld:C0280100
;
a
sio:SIO_001121
.
}
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_provenance
{
dgn-np:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_assertion
dcterms:description
"[Recently, we have cloned and characterized the Ras association domain family 1A gene (RASSF1A) at 3p21.3, from which loss of genetic material is one of the most frequent events in several types of human solid tumors.]. 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:12360410
;
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:NP793919.RAxwgHcqjitF9iwwo4ALq98ljQi3VXb9w-EQ-fQyqZWrw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}