Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.
- NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_assertion description "[We investigated BTK gene expression in an XLA/GHD patient from the family originally described by Northern analysis, cDNA sequencing, and Western analysis of protein production using mAb to BTK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.
- NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_assertion evidence source_evidence_literature NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.
- NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_assertion SIO_000772 7650402 NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.
- NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_assertion wasDerivedFrom befree-2016 NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.
- NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_assertion wasGeneratedBy ECO_0000203 NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1316516.RAsnBv8CLSM53hKjU0UDvHBkClbW2wPEZkIcXYQgIo2_U130_provenance.