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- source_evidence_literature type ECO_0000212 NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.
- NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_assertion description "[However, the function of GPR56 remained unclear until 2004 when mutations in the human GPR56 gene were found to cause a specific brain malformation called bilateral frontoparietal polymicrogyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.
- NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_assertion evidence source_evidence_literature NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.
- NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_assertion SIO_000772 20374731 NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.
- NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_assertion wasDerivedFrom befree-2016 NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.
- NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_assertion wasGeneratedBy ECO_0000203 NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.
- befree-2016 importedOn "2016-02-19" NP804754.RAjf9nEFYcbm0tjdsDC4WSM3w_cTOMBDlMb2HPG7pCKbo130_provenance.