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- source_evidence_literature type ECO_0000212 NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.
- NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_assertion description "[We found a high incidence of ASXL1 mutation in MF patients (20%) and a low incidence in PV (7%) and ET (4%) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.
- NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_assertion evidence source_evidence_literature NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.
- NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_assertion SIO_000772 22489043 NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.
- NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_assertion wasDerivedFrom befree-2016 NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.
- NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_assertion wasGeneratedBy ECO_0000203 NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.
- befree-2016 importedOn "2016-02-19" NP973594.RA1sWNFi1c5U0MDVQMJFy4m5p65AxfkmqwBJWy3d6rjXw130_provenance.