Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.
- NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_assertion description "[Using a probe that detects a polymorphic locus within the RB1 gene we found loss of only one allele (heterozygous deletion) in 33% of soft tissue sarcomas examined, including two leiomyosarcomas, a malignant peripheral nerve sheath tumour, a rhabdomyosarcoma and a chondrosarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.
- NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_assertion evidence source_evidence_literature NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.
- NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_assertion SIO_000772 2765366 NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.
- NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_assertion wasDerivedFrom befree-2016 NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.
- NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_assertion wasGeneratedBy ECO_0000203 NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296639.RAQ0quoHkBT2B4_30hA8ZoVWFARRQx2AEYS7q1Ulr4ZAg130_provenance.