Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.
- NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_assertion wasGeneratedBy ECO_0000218 NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.
- NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_assertion wasDerivedFrom ctd_human-20130708 NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.
- NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_assertion SIO_000772 21091464 NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.
- NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_assertion evidence source_evidence_curated NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.
- NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_assertion description "[Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP27502.RAQeF-0F3v1oxlfk6EsFHkj3-4E97JfXLasiz-t6pa-48130_provenance.