Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.
- NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_assertion description "[More rarely, it occurs in the Li-Fraumeni syndrome, caused by a p53 germline mutation, in which markedly early-onset BC is found in association with brain tumors, sarcomas, leukemia, lymphoma, malignant melanoma, and adrenal cortical carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.
- NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_assertion evidence source_evidence_literature NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.
- NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_assertion SIO_000772 18086272 NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.
- NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_assertion wasDerivedFrom befree-20140225 NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.
- NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_assertion wasGeneratedBy ECO_0000203 NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP280495.RA6GfEn8mGJ37WoheTtUFy6Su4X42Ah_UseuTQcxFymtE130_provenance.