Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_assertion> ?p ?o ?g. }
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- NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_assertion type Assertion NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_head.
- NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_assertion description "[A further two cases include a father and a daughter, both of whom are suffering from NSCLC with different EGFR mutation patterns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_provenance.
- NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_assertion evidence source_evidence_literature NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_provenance.
- NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_assertion SIO_000772 24754584 NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_provenance.
- NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_assertion wasDerivedFrom befree-2016 NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_provenance.
- NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_assertion wasGeneratedBy ECO_0000203 NP1175644.RACd-j6WCsMhH6jHHaRVgSfhx9OfTOrKypdEqNq-RnpT8130_provenance.