Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1158122.RAploYJtFHQ7y-YMRnNh1wUTChouLfU2MQTtEtlCqcbSU130_provenance.