Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_assertion type Assertion NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_head.
- NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_assertion description "[Hypophosphatasia (HPP) is a clinically heterogeneous rare, inherited disorder of bone and mineral metabolism with extensive allelic heterogeneity in the ALPL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.
- NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_assertion evidence source_evidence_literature NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.
- NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_assertion SIO_000772 24569605 NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.
- NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_assertion wasDerivedFrom befree-2016 NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.
- NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_assertion wasGeneratedBy ECO_0000203 NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.