Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.
- NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_assertion description "[The phenotype and allele frequencies of the four gene loci (AB0, RH, PTC and colour blindness) show considerable differences between these populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.
- NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_assertion evidence source_evidence_literature NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.
- NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_assertion SIO_000772 14524000 NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.
- NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_assertion wasDerivedFrom befree-2016 NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.
- NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_assertion wasGeneratedBy ECO_0000203 NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.
- befree-2016 importedOn "2016-02-19" NP415670.RA6AxAAnSDr5VMKU7AdEZa3JVLfN5Ayr2TGGJZX4oSpgw130_provenance.