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- source_evidence_literature type ECO_0000212 NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.
- NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_assertion description "[This is the first description of a family with two SCA mutations with affected subjects having a combined SCA2 and SCA10 phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.
- NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_assertion evidence source_evidence_literature NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.
- NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_assertion SIO_000772 25630585 NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.
- NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_assertion wasDerivedFrom befree-2016 NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.
- NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_assertion wasGeneratedBy ECO_0000203 NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259137.RAlDyiHi-fpXDtZX204RWAnxaPXK_a3UcsYLD6Iow4WOM130_provenance.