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- source_evidence_literature type ECO_0000212 NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.
- NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_assertion description "[The copy number variation of erbB2 gene from plasma can be used as prognostic marker for early detection of patients at risk of worse clinical outcome in esophageal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.
- NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_assertion evidence source_evidence_literature NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.
- NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_assertion SIO_000772 21481261 NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.
- NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_assertion wasDerivedFrom befree-2016 NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.
- NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_assertion wasGeneratedBy ECO_0000203 NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.
- befree-2016 importedOn "2016-02-19" NP886107.RAr5Qu8aHJtp_tFktxzCc4tjQSdeAdVYL92BPU2_6NlSI130_provenance.