Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.
- NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_assertion description "[Four of nine informative fetal rhabdomyomas and embryonal rhabdomyosarcomas showed loss of heterozygosity (LOH) in the PTCH region with two of these (one fetal rhabdomyoma and one embryonal rhabdomyosarcoma) also showing LOH in the SUFU region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.
- NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_assertion evidence source_evidence_literature NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.
- NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_assertion SIO_000772 16294371 NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.
- NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_assertion wasDerivedFrom befree-20150227 NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.
- NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_assertion wasGeneratedBy ECO_0000203 NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP907558.RA_-Vrw0hqBkoIPUDlSg8Om2lfj8tqpHBbdM6qkN56uB8130_provenance.