Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.
- NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_assertion wasGeneratedBy ECO_0000203 NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.
- NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_assertion wasDerivedFrom befree-20140225 NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.
- NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_assertion SIO_000772 1348049 NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.
- NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_assertion evidence source_evidence_literature NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.
- NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_assertion description "[During a systematic chromosomal survey of 167 unrelated boys with the X-linked recessive Menkes disease (MIM 309400), a unique rearrangement of the X chromosome was detected, involving an insertion of the long arm segment Xq13.3-q21.2 into the short arm at band Xp11.4, giving the karyotype 46,XY,ins(X) (p11.4q13.3q21.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP928779.RAayCVPoHvJONZDgh2Wkc10Bdtzgk96pnlxuAPKxe9quA130_provenance.