Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.
- NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_assertion description "[DCX mutations usually cause anteriorly predominant lissencephaly in male patients and subcortical band heterotopia in female patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.
- NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_assertion evidence source_evidence_literature NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.
- NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_assertion SIO_000772 15921228 NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.
- NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_assertion wasDerivedFrom befree-2016 NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.
- NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_assertion wasGeneratedBy ECO_0000203 NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.
- befree-2016 importedOn "2016-02-19" NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_provenance.