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- source_evidence_literature type ECO_0000212 NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.
- NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_assertion description "[Our study illustrates that if only a single heterozygous SLC26A4/PDS mutation is found in a patient with goiter and deafness, other genetic explanations should be considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.
- NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_assertion evidence source_evidence_literature NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.
- NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_assertion SIO_000772 16684826 NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.
- NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_assertion wasDerivedFrom befree-20150227 NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.
- NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_assertion wasGeneratedBy ECO_0000203 NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP655311.RAnmDyYLDukDYwWJRP9elIl2nz3YEOTuIjyBLXzWRPS7o130_provenance.