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- source_evidence_literature type ECO_0000212 NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.
- NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_assertion description "[We demonstrate its use in identifying ARTN as a strong candidate gene within the 1p34.1-p32 mapped locus for a hereditary form of ptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.
- NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_assertion evidence source_evidence_literature NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.
- NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_assertion SIO_000772 22331800 NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.
- NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_assertion wasDerivedFrom befree-20140225 NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.
- NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_assertion wasGeneratedBy ECO_0000203 NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697531.RAa_k20OM93I10cWE6SBR2kEu2DoTaUwQce3dZsxD-qrs130_provenance.