Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.
- NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_assertion description "[We used massively parallel sequencing to examine tumor samples collected from 87 patients with MDS before HSCT for coding mutations in 40 recurrently mutated MDS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.
- NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_assertion evidence source_evidence_literature NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.
- NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_assertion SIO_000772 25092778 NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.
- NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_assertion wasDerivedFrom befree-20150227 NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.
- NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_assertion wasGeneratedBy ECO_0000203 NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781442.RAKba7MMvHMmYU-bU2r68UlaEV29JS4aKHr1A_W6GmZ_E130_provenance.