Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.
- NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_assertion wasGeneratedBy ECO_0000218 NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.
- NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_assertion wasDerivedFrom uniprot-20150221 NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.
- NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_assertion SIO_000772 20890278 NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.
- NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_assertion evidence source_evidence_curated NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.
- NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_assertion description "[Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212.RAbuEEOEDlm3Q-lqG1GwkI_iGafaSK3aA2dE6ne0xGAhs130_provenance.