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- source_evidence_literature type ECO_0000212 NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.
- NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_assertion description "[Genetic testing allows familial counseling and identifies subjects at high risk of malignancy (SDHB mutations) or significant multiorgan disease (RET, VHL, or NF1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.
- NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_assertion evidence source_evidence_literature NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.
- NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_assertion SIO_000772 20236688 NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.
- NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_assertion wasDerivedFrom befree-2016 NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.
- NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_assertion wasGeneratedBy ECO_0000203 NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP800575.RAACyeHJPYEnydc10kqsB1RaxFygUITdW6DJYmhwc_DIQ130_provenance.