Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.
- NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_assertion wasGeneratedBy ECO_0000203 NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.
- NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_assertion wasDerivedFrom befree-20140225 NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.
- NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_assertion SIO_000772 15160522 NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.
- NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_assertion evidence source_evidence_literature NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.
- NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_assertion description "[Loss of heterozygosity in the 9p21-p22 region, has been frequently described in a wide range of human malignancies, including familial melanomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697555.RA6nkjThWiMuD4Qi2_DX5mV5Q1f5UL8VoaCdjLo9tCU6Y130_provenance.