Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.
- NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_assertion description "[Mutational screening of these genes by means of Denaturing High Performance Liquid Chromatography (DHPLC) in breast and/or ovarian cancer-prone families from Southern Germany revealed 15 novel BRCA1 and 8 novel BRCA2 sequence variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.
- NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_assertion evidence source_evidence_literature NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.
- NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_assertion SIO_000772 12938098 NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.
- NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_assertion wasDerivedFrom befree-2016 NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.
- NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_assertion wasGeneratedBy ECO_0000203 NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.
- befree-2016 importedOn "2016-02-19" NP406609.RAbI4uW4PsXIzjxpM-q12CANOUtGI_st32oaTAUNfy1gI130_provenance.