Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.
- NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_assertion description "[Exome sequencing identifies GRIN2A as frequently mutated in melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.
- NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_assertion evidence source_evidence_curated NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.
- NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_assertion SIO_000772 21499247 NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.
- NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_assertion wasDerivedFrom ctd_human-2016 NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.
- NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_assertion wasGeneratedBy ECO_0000218 NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP29078.RAzhHT9fD8E9UDHP33o3Dqev1_fvKkSWYJW5Jwv-5KoFo130_provenance.