Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.
- NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_assertion description "[It is important to determine the STS activity in the propositus mother of apparently non familial cases of XLI to identify the carrier state and provide and accurate genetic counseling, as most of these seem to correspond to inherited cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.
- NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_assertion evidence source_evidence_literature NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.
- NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_assertion SIO_000772 7546451 NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.
- NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_assertion wasDerivedFrom befree-2016 NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.
- NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_assertion wasGeneratedBy ECO_0000203 NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.
- befree-2016 importedOn "2016-02-19" NP1312019.RAIp9J8epbht9gjPXp5gIvhNGfHyHrvWrmeB2NPDmB2ME130_provenance.