Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_assertion> ?p ?o ?g. }
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- NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_assertion type Assertion NP496789.RAj_yhvoW2KRYbry9JU8GxyJgaM0ASGO0A4V4bDt_QLTA130_head.
- 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.