Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.
- NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_assertion description "[The aim of this study was to identify this phenotype amongst index cases from families in the kConFab familial breast cancer resource with no known pathogenic mutation ('BRCAX' families).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.
- NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_assertion evidence source_evidence_literature NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.
- NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_assertion SIO_000772 18446624 NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.
- NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_assertion wasDerivedFrom befree-2016 NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.
- NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_assertion wasGeneratedBy ECO_0000203 NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP668600.RALWcPqr3A1ZMec0fFdySxkSe9U_Vvv0e8NZ7ru5GlUKw130_provenance.