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- source_evidence_literature type ECO_0000212 NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.
- NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_assertion description "[VCP mutations are a rare cause of familial ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.
- NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_assertion evidence source_evidence_literature NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.
- NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_assertion SIO_000772 22078486 NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.
- NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_assertion wasDerivedFrom befree-20150227 NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.
- NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_assertion wasGeneratedBy ECO_0000203 NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768725.RAnvyV2nkkRfYdh-U2vLc8qEqGycsvDapwt3gdo95KTx4130_provenance.