Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.
- NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_assertion description "[Alterations of known genes in PRCC include missense mutations in the MET oncogene (7q31) and rare translocations fusing TFE3 at Xp11.2 with a variety of other loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.
- NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_assertion evidence source_evidence_literature NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.
- NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_assertion SIO_000772 12213728 NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.
- NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_assertion wasDerivedFrom befree-20150227 NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.
- NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_assertion wasGeneratedBy ECO_0000203 NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP554468.RA-rD_PPV-WK9ySTRiLkHXKWx1Qopqk_1sdOUZaONhCVg130_provenance.