Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.
- NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_assertion description "[In a second series, we screened 140 patients with MR and behaviour disturbance who did not fulfil the de Vries criteria for subtelomeric rearrangements and who had a normal karyotype and no detectable FRAXA mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.
- NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_assertion evidence source_evidence_literature NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.
- NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_assertion SIO_000772 16773131 NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.
- NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_assertion wasDerivedFrom befree-2016 NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.
- NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_assertion wasGeneratedBy ECO_0000203 NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.
- befree-2016 importedOn "2016-02-19" NP554495.RAzxVdvOm6E3McQxeZyT5aILaQ_gbKzNN0D_g6GM0S7-k130_provenance.