Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.
- NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_assertion description "[The macular hypoplasia has to be considered a concerted interaction with compound heterozygous mutations in the P gene manifesting a mild form of oculocutaneous albinism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.
- NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_assertion evidence source_evidence_literature NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.
- NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_assertion SIO_000772 16453125 NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.
- NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_assertion wasDerivedFrom lhgdn-20090331 NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.
- NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_assertion wasGeneratedBy ECO_0000203 NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP152553.RAow61OVlbDPX_De03tRJTMMEvJQa_q2vcwLnPFrvUhYw130_provenance.