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- source_evidence_literature type ECO_0000212 NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.
- NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_assertion description "[A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.
- NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_assertion evidence source_evidence_literature NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.
- NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_assertion SIO_000772 20850105 NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.
- NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_assertion wasDerivedFrom befree-2016 NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.
- NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_assertion wasGeneratedBy ECO_0000203 NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.
- befree-2016 importedOn "2016-02-19" NP839970.RA-26RngjDNrakkNPtwDl9kdZm5umHqR308OgiV72vhtk130_provenance.