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- source_evidence_literature type ECO_0000212 NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.
- NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_assertion description "[None of the GSD Ia HCA had biallelic mutations in the HNF1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.
- NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_assertion evidence source_evidence_literature NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.
- NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_assertion SIO_000772 19762333 NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.
- NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_assertion wasDerivedFrom befree-2016 NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.
- NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_assertion wasGeneratedBy ECO_0000203 NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.
- befree-2016 importedOn "2016-02-19" NP763938.RAQuYw-T6e5RS1qDQSoBvMjXdrwC1BW6w4F19m4-yP1ig130_provenance.