Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.
- NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_assertion description "[The clinical concomitant is a severe, G-CSF-responsive neutropenia in addition to oculocutaneous albinism and platelet storage pool deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.
- NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_assertion evidence source_evidence_literature NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.
- NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_assertion SIO_000772 11809908 NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.
- NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_assertion wasDerivedFrom befree-20140225 NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.
- NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_assertion wasGeneratedBy ECO_0000203 NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP763100.RAp7X3_SRE2wiVGig2BWLiL2repnLMMCJ8HV5qTIUna9A130_provenance.