Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.
- NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_assertion description "[Cytogenetic and molecular cytogenetic studies have identified multiplication of 12p, manifested in i(12p) or tandem duplication of 12p, as a unique change in GCTs which serves as a diagnostic marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.
- NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_assertion evidence source_evidence_literature NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.
- NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_assertion SIO_000772 9562446 NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.
- NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_assertion wasDerivedFrom befree-20150227 NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.
- NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_assertion wasGeneratedBy ECO_0000203 NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.
- befree-20150227 importedOn "2015-02-27" NP891228.RAA1kP40C7mM-_MqVsgda4LBQ5SSbxy_sHom7-flgciws130_provenance.