Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.
- NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_assertion description "[Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.
- NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_assertion evidence source_evidence_curated NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.
- NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_assertion SIO_000772 23603762 NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.
- NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_assertion wasDerivedFrom ctd_human-2016 NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.
- NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_assertion wasGeneratedBy ECO_0000218 NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP32870.RAVccs1jLWo7tK-pyMoaIS3SYx3cYwl3Uvo0DapQd6n2Q130_provenance.