Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.
- NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_assertion description "[The X-linked transmission hypothesis has been tested by using several markers on chromosome X: Xg blood group, colour blindness, glucose-6-phosphate dehydrogenase (G6PD), factor IX (haemophilia B), and DNA probes such as DXS15, DXS52, F8C, ST14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.
- NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_assertion evidence source_evidence_literature NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.
- NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_assertion SIO_000772 8423707 NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.
- NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_assertion wasDerivedFrom befree-20140225 NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.
- NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_assertion wasGeneratedBy ECO_0000203 NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP902387.RAB16i0gdMy9luWQED4JJbKSNGyBmepMHA_-LkhVQlUgI130_provenance.